Home NDC 87510-001 Amerfresh Medicated Body Powder
Product NDC 87510-001
11-digit product format 875100001
Labeler code 87510
Product ID 87510-001_5cb83d87-75a4-ca97-e063-6394a90ad098
Type HUMAN OTC DRUG
Nonproprietary name Menthol and Zinc Oxide
Dosage form POWDER
Route TOPICAL
Labeler ONEST LIMITED
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-04-25
Marketing end 2027-10-01
Substance MENTHOL; ZINC OXIDE
Active strength .15; 1 g/100g; g/100g
NDC exclude flag No
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Amerfresh Medicated Body Powder Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL .15 g/100g ZINC OXIDE 1 g/100g
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87510-001-01 Amerfresh Medicated Body Powder 285 g in 1 BOTTLE POWDER 285 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 38 of 68 · 1,350 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 87510-001-01 87510000101 285 g in 1 BOTTLE (87510-001-01) 285 g 2026-04-25 2027-10-01 No No Historical