OEM / private label · the United States
Body care OEM / private label manufacturing for the United States
BIOSPHERE runs 15 automated lines under GMPC / ISO 22716 / HALAL / FDA / EU CPNP / SGS, holds 27 proven body care formulations and 2819 stock packaging options for this category. For the United States, products enter the market through U.S. Food and Drug Administration (FDA); the filing route, responsible-person rule and label language are summarised below from the official texts. Commercial terms are quoted per project in writing.
Factory-side digest of the official texts; the official text prevails; not legal advice.
What the United States requires before sale
- Market entry
- No pre-market approval — MoCRA requires facility registration (renewed every two years) and product listing (updated annually) through FDA's Cosmetics Direct portal, enforced since 2024-07-01; color additives need FDA approval and sunscreens/anti-dandruff products are OTC drugs.
- Responsible person
- A 'responsible person' is the manufacturer, packer or distributor whose name appears on the label; a U.S. address is not mandated, but foreign facilities must name a U.S. agent and the responsible person must handle adverse-event reporting.
- Labeling
- English labelling per 21 CFR 701 and the FPLA (identity, net contents, ingredients in descending order, warnings, responsible person name/address); MoCRA adds a domestic address/phone or e-mail for adverse-event contact and professional-use statements; fragrance-allergen disclosure starts only once FDA's pending rule is final.
- Official source
- https://www.fda.gov/cosmetics/cosmetics-laws-regulations/modernization-cosmetics-regulation-act-2022-mocra
What is on file for body care
27 proven body care formulations on file (formats: body-lotion · lotion · body-spray · gel · hand-cream · scrub), plus 2819 stock packaging options in the formats this category uses. Numbers are live counts from the formulation and packaging libraries on this site.
How a project runs
Brief → base selection or new formulation → sample (usually 5–14 days) → stability (40C accelerated) and preservative challenge (ISO 11930 / USP <51>) → packaging compatibility → dossier for U.S. Food and Drug Administration (FDA) → production on the certified lines → label review before shipment.
FAQ
Can BIOSPHERE manufacture body care products for a US brand?
Yes. 27 body care formulations are on file, produced on 15 automated lines under GMPC / ISO 22716 / HALAL / FDA / EU CPNP / SGS; the dossier is prepared for U.S. Food and Drug Administration (FDA).
Who files the product in the United States?
A 'responsible person' is the manufacturer, packer or distributor whose name appears on the label
What must the label carry in the United States?
English labelling per 21 CFR 701 and the FPLA (identity, net contents, ingredients in descending order, warnings, responsible person name/address)
What are the MOQ, sampling time and price?
Sampling usually takes 5–14 days from brief confirmation to dispatch (existing bases at the short end, new formulations at the long end). MOQ and price depend on the format, whether the packaging is a stock shape or a new mould, and whether the formula changes; they are stated per project in a written quotation.
Related buyer questions
- Body lotion and body wash OEM for the United States: how are fragrance allergens and labeling handled?
- We are promoting a Retinol eye cream on Amazon US with the text 'clinically proven' and 'dramatically reduces wrinkles.' If complained about by professional complainers, can the factory provide efficacy substantiation files compliant with FTC standards and a response strategy?
- Shampoo and conditioner OEM for the United States: what matters in a sulfate-free formula and on the label?
- Launching a skincare product (serum or cream) in the United States: what does the OEM factory need to prepare, and how long does notification take?
- Lip gloss and foundation OEM for the United States: how are colourant lists and heavy-metal limits met?
- What is the difference between MoCRA compliance and routine GMPC audits in US cosmetics manufacturing, and how should a factory prepare for inspections?
Planning a body care line for the United States? Send the product type and target launch; we reply with the filing checklist and a written quotation. Send an inquiry