Home NDC 70157-026 Silk Mineral SPF 50 Sunscreen Face
Product NDC 70157-026
11-digit product format 701570026
Labeler code 70157
Product ID 70157-026_5e48fd72-46df-daa7-e063-6394a90adef8
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler Baxter Laboratories
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-05-09
Substance ZINC OXIDE
Active strength 20 g/100mL
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 Silk Mineral SPF 50 Sunscreen Face
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 20 g/100mL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70157-026-01 Silk Mineral SPF 50 Sunscreen Face 50 mL in 1 BOTTLE LOTION 50 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70157-026 SILK MINERAL SPF 50 SUNSCREEN FACE (ZINC OXIDE) LOTION [BAXTER LABORATORIES] 1 Current NDC, 1 package rows 20250509_33ddaac7-925e-259c-e063-6294a90a120c.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 162 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 70157-026-01 70157002601 50 mL in 1 BOTTLE (70157-026-01) 50 ml 2025-05-09 No No Current