Home NDC 87170-006 Zinc Oxide 20%
Product NDC 87170-006
11-digit product format 871700006
Labeler code 87170
Product ID 87170-006_4960925b-fe36-43b0-e063-6394a90a42cc
Type HUMAN OTC DRUG
Nonproprietary name Sunscreen SPF 50 Mineral
Dosage form LOTION
Route TOPICAL
Labeler S&C Hampton Sun
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-10-09
Substance ZINC OXIDE
Active strength 20 g/100mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag No
Listing certified through 2027-12-31
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 Zinc Oxide 20%
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 20 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87170-006-10 Zinc Oxide 20% 946 mL in 1 BOTTLE LOTION 946 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 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87170-006-10 87170000610 946 mL in 1 BOTTLE (87170-006-10) 946 ml 2025-10-09 No No Current