Home NDC 87702-409 Elaine Sterling Hydrating Sunscreen
Product NDC 87702-409
11-digit product format 877020409
Labeler code 87702
Product ID 87702-409_547a001e-f2a8-b16e-e063-6394a90a1e42
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form CREAM
Route TOPICAL
Labeler Elaine Sterling Enterprises
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-10-01
Substance ZINC OXIDE
Active strength 21 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 Elaine Sterling Hydrating Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 21 g/100g
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.
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 242 of 353 · 7,041 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87702-409-01 87702040901 50 g in 1 BOTTLE, DISPENSING (87702-409-01) 50 g 2024-10-01 No No Current