Home NDC 21130-751 Open Nature Zinc Oxide Sunscreen Mineral Sunscreen SPF 30
Product NDC 21130-751
11-digit product format 211300751
Labeler code 21130
Product ID 21130-751_247797c9-5b6e-3d2d-e063-6394a90a9009
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 182.4 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 Zinc Oxide Sunscreen Mineral Sunscreen SPF 30
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 182.4 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 21130-751-09 Open Nature Zinc Oxide Sunscreen Mineral Sunscreen SPF 30 89 mL in 1 TUBE LOTION 89 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 21130-751 OPEN NATURE ZINC OXIDE SUNSCREEN MINERAL SUNSCREEN SPF 30 (ZINC OXIDE) LOTION [SAFEWAY, INC.] 2 Current NDC, Legacy NDC, 1 package rows 20241016_dbeff8e8-250d-8274-e053-2995a90a984e.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 21130-751-09 21130075109 89 mL in 1 TUBE (21130-751-09) 89 ml 2018-12-05 0000-00-00 No No Current