Field notes on making and moving product
Field notes from PMG on product development, contract manufacturing, MOQs, certifications, and channel strategy.
Turnkey or Consigned Ingredients? Should You Supply Your Own Raw Materials to a Supplement or Skincare Manufacturer?
Published
Turnkey vs consigned ingredients for supplement and skincare brands: what FDA's GMP rules require, hidden costs, and a 10-point readiness checklist.
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What Should You Send a Contract Manufacturer to Get an Accurate Quote? A Product Brief Checklist for Supplement and Skincare Brands
Published
The 9-line product brief for an accurate supplement or skincare manufacturing quote: claims, quantity, packaging, testing, channels and budget.
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How Do You Price a Private Label Supplement or Skincare Product? Cost per Unit, Margins for Amazon, Retail and DTC
Published
Turn your cost per unit into a shelf price: what you keep on Amazon, your own site and in retail, keystone vs margin, and a pricing checklist.
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What Happens If Your Private Label Supplement or Skincare Product Has to Be Recalled? Lot Codes, FDA Recall Classes and a Recall-Ready Checklist
Published
What happens if your private label supplement or skincare product is recalled: FDA recall classes, lot code rules, who acts and a recall-ready checklist.
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Can You Put “Made in USA” on a Private Label Supplement or Skincare Product? The FTC’s “All or Virtually All” Test, Qualified Claims and a Checklist
Published
Can a private label supplement or skincare product say Made in USA? The FTC’s 3-part test, qualified claims, California’s rule and a sourcing checklist.
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What Changes When You Scale a Private Label Supplement or Skincare Product From Your First Run to 10,000+ Units?
Published
What changes when you scale a private label supplement or skincare product past your first run: batch records, FDA listings, lead times and per-unit cost.
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Can a Spa or Med Spa Launch Its Own Private Label Skincare Line? Claims, Labels, MoCRA Rules and Minimums
Published
How a spa or med spa launches its own skincare line: which claims make it a drug, what the label needs under MoCRA, professional-use rules and PMG minimums.
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Capsules, Tablets or Stick Packs? How to Choose a Private Label Supplement Format (Minimums, Testing and Label Rules)
Published
Capsules, tablets or stick packs (sachets)? Compare minimums (from 1,000 units at PMG, varies by format), label wording, testing and FDA rules before choosing a format.
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What Do Retailers Require Before They Stock Your Private Label Supplement or Skincare Product? Barcodes, Insurance, Testing and Audits
Published
Barcodes, liability insurance, FDA filings, test results and routing guides: the 6 checks retailers run before stocking your private label product.
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Does Your Private Label Supplement or Skincare Product Need a Prop 65 Warning? Who Decides, What It Says and the 2025 Short-Form Rules
Published
Does your private label supplement or skincare product need a Prop 65 warning? Who's responsible, what it must say, the 2025 short-form rules and a checklist.
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How Long Does Stability Testing Take for a Private Label Skincare Product? Accelerated vs Real-Time, Challenge Tests and Shelf Life
Published
Accelerated stability testing typically runs about 3 months at PMG, with real-time testing to confirm shelf life. What cosmetics and OTC drugs need.
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What Should a Supplement Certificate of Analysis (COA) Show? A Line-by-Line Guide for Private Label Brands
Published
What a supplement certificate of analysis must show under 21 CFR 111: methods, limits, actual results, identity and heavy metals, plus a printable checklist.
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Which Certifications Should a Supplement or Skincare Manufacturer Have? cGMP, NSF, USP, Organic, Kosher and Halal Explained
Published
Certifications a supplement or skincare maker needs: what FDA requires, what NSF, USP and ISO 22716 audits prove, and organic, kosher, halal rules.
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What Has to Be on a Private Label Supplement Label? Supplement Facts, Claims, Disclaimer and Allergens
Published
What a private label supplement label must include: 5 required statements, Supplement Facts rules, the claims disclaimer, allergens and adverse event contact.
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Who Is the Responsible Person Under MoCRA When You Private Label a Cosmetic?
Published
Under MoCRA, the company named on a private label cosmetic's label is the responsible person. See who registers, lists and reports adverse events.
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Is Your Massage Oil or Muscle Rub a Cosmetic or an OTC Drug?
Published
When a massage oil becomes an OTC drug: claims, FDA M017 menthol and camphor levels, child-resistant packaging, Drug Facts, minimums and timelines.
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Can You Private Label Hotel Amenities? Body Wash, Shampoo and Lotion for Boutique Hotels and Spas
Published
How boutique hotels and spas private label body wash, shampoo and lotion: minimums, timelines, state small-bottle laws and what the label must include.
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What Is a Pilot Batch, and Can Your First Production Run Be Under 1,000 Units?
Published
Lab sample vs pilot batch vs first production run, why tiny runs cost more per unit, six realistic options below 1,000 units, and a downloadable readiness checklist.
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Can You Private Label Essential Oils and Aromatherapy Kits for Amazon?
Published
How claims set the FDA category, what Amazon hazmat review needs, when caps must be child-resistant, and PMG's minimums.
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Can You Make Sugar-Free Pectin Gummies with Allulose?
Published
How the gel changes without sugar, allulose vs sugar alcohols vs monk fruit and stevia, what a sugar-free label needs, and realistic minimums.
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What Does It Take to Manufacture an OTC Acne Product?
Published
When an acne product becomes an OTC drug, which actives and strengths FDA’s acne monograph allows, Drug Facts labeling, NDCs and registration, what changes on the manufacturing floor, and realistic MOQs and timelines — plus a downloadable launch checklist.
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How to Choose a Private Label Manufacturing Partner: 10 Questions Every Brand Should Ask
Published
Certifications, category experience, quality control, scaling, MOQs and lead times, IP, cost transparency, communication, scope of service, and what happens when things go wrong — plus a downloadable evaluation checklist.
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How Much Does It Cost to Manufacture Supplements? 2026 Breakdown
Published
A phase-by-phase look at R&D, ingredients, production, packaging, and compliance costs — plus total first-batch investment for private label and custom formulation.
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MOQ and Manufacturing Volume: What Actually Matters (And Why Your Numbers Might Be Wrong)
Published
Why minimums exist, how they shift by category and development path, the costs that appear when volume is too low, and how to negotiate a first run you can actually sell through.
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