U.S. OTC Products

U.S. OTC Product Development & Manufacturing

Explore product-specific development and manufacturing pathways for applicable U.S. OTC categories.

U.S. OTC Products
U.S. OTC Products
Development Options

Develop Products for the U.S. OTC Market

Explore product development and manufacturing pathways for applicable OTC categories, including sunscreen, anti-acne and anti-dandruff products.

Category-Specific Development
Evaluate the intended use and applicable product classification.
Formula & Label Review
Discuss active ingredients, claims, labeling and required documentation.
Manufacturing Coordination
Align formulation, testing, packaging and production requirements.
Regulatory Planning
Clarify applicable U.S. OTC requirements for the individual product.
Customization Options

Customize Your Product From Formula to Packaging

Every brand has different product goals, target customers and packaging preferences. Longway works with your team to explore suitable formulation directions, product formats and packaging options based on your project requirements.

Formula Development

Discuss ingredients, texture, fragrance and product performance goals.

Packaging Solutions

Explore suitable containers, pumps, caps, cans and dispensing formats.

Branding & Labeling

Coordinate product appearance, label design and brand artwork.

Sample Evaluation

Review sample requirements, product specifications and packaging compatibility.

Manufacturing & Quality

From Product Development to Scalable Manufacturing

Longway combines product development, manufacturing coordination and quality-focused production processes to support private label projects from initial discussions to production preparation.

Longway cleanroom production line for cosmetic OEM ODM manufacturing
Manufacturing Infrastructure
Explore our manufacturing facilities, production lines, and equipment for cosmetic product development and OEM/ODM manufacturing.
Production Processes
From filling and packaging to production planning, our processes are coordinated to support product specifications and project requirements.
Quality Control
Quality checks cover raw materials, in-process controls, and finished product testing according to applicable procedures and product requirements.
Documentation & Compliance
We coordinate relevant product documentation and regulatory requirements according to product category, target market, and project scope.
FAQ

Frequently Asked Questions About U.S. OTC Products Private Label Manufacturing

Common questions to help prepare a more complete product inquiry.

What types of OTC products can you support?
Discuss eligible categories such as sunscreen, acne products, dandruff treatments, antiperspirants, and skin protectants, subject to verified capabilities.
What is required to develop an OTC product for the U.S. market?
Requirements depend on the product category, applicable monograph or order, ingredients, labeling, and manufacturing arrangements.
Can you help with Drug Facts labeling and product documentation?
Relevant documentation and labeling coordination can be discussed based on the product and the agreed scope of service. U.S. OTC products must follow applicable labeling requirements.
Does FDA facility registration mean a product is FDA approved?
No. Facility registration or listing does not itself mean FDA has approved a facility or every product it manufactures.

Ready to Develop Your Private Label Beauty Products?

Tell us about your product direction, target market, packaging preferences and estimated order quantity. Our team can review your requirements and discuss the next steps for your OEM/ODM project.