Home NDC 82516-202 Sunscreen
Product NDC 82516-202
11-digit product format 825160202
Labeler code 82516
Product ID 82516-202_5d5afcd4-f625-1117-e063-6394a90a2116
Type HUMAN OTC DRUG
Nonproprietary name Everyday Skin Tint SPF 30
Dosage form LOTION
Route TOPICAL
Labeler True Botanicals
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-06-16
Substance ZINC OXIDE
Active strength 18 g/100g
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 Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 18 g/100g
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 82516-202-01 Sunscreen 30 g in 1 BOTTLE, PUMP LOTION 30 4 82516-202-02 Sunscreen 1 in 1 CARTON LOTION 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82516-202 SUNSCREEN (EVERYDAY SKIN TINT SPF 30) LOTION [TRUE BOTANICALS] 3 Current NDC, Legacy NDC, 2 package rows 20241105_e17ee943-8f6f-630d-e053-2995a90ae40e.zip
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 Marketing end Sample Exclude flag Status 82516-202-01 82516020201 30 g in 1 BOTTLE, PUMP 30 g Historical 82516-202-02 82516020202 1 BOTTLE, PUMP in 1 CARTON (82516-202-02) / 30 g in 1 BOTTLE, PUMP (82516-202-01) 2022-06-16 0000-00-00 No No Current