Home NDC 37808-350 HEB Sensitive 50 Mineral Sensitive Skin Sunscreen For Face
Product NDC 37808-350
11-digit product format 378080350
Labeler code 37808
Product ID 37808-350_2489cda6-c2f2-a801-e063-6394a90af088
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler H.E.B.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-01-28
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 HEB Sensitive 50 Mineral Sensitive Skin Sunscreen For Face
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 37808-350-09 HEB Sensitive 50 Mineral Sensitive Skin Sunscreen For Face 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 37808-350 HEB SENSITIVE 50 MINERAL SENSITIVE SKIN SUNSCREEN FOR FACE (ZINC OXIDE) LOTION [H.E.B.] 2 Current NDC, Legacy NDC, 1 package rows 20241017_dfb43fc5-4968-f999-e053-2a95a90a0819.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 37808-350-09 37808035009 89 mL in 1 TUBE (37808-350-09) 89 ml 2021-01-28 0000-00-00 No No Current