Home NDC 21130-725 OPEN NATURE CHILDREN SPF 50 MINERAL SUNSCREEN
Product NDC 21130-725
11-digit product format 211300725
Labeler code 21130
Product ID 21130-725_24772245-f75e-9c5c-e063-6394a90a8a63
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler SAFEWAY, INC.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-12-05
Substance ZINC OXIDE
Active strength 216 mg/mL
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 OPEN NATURE CHILDREN SPF 50 MINERAL SUNSCREEN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 216 mg/mL
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 21130-725-03 OPEN NATURE CHILDREN SPF 50 MINERAL SUNSCREEN 89 mL in 1 TUBE LOTION 89 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 21130-725 OPEN NATURE CHILDREN SPF 50 MINERAL SUNSCREEN (ZINC OXIDE) LOTION [SAFEWAY, INC.] 3 Current NDC, Legacy NDC, 1 package rows 20241016_a6044f0f-eb86-684d-e053-2995a90a0921.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 21130-725-03 21130072503 89 mL in 1 TUBE (21130-725-03) 89 ml 2018-12-05 0000-00-00 No No Current