Home NDC 71501-1904 Dr Loretta Universal Glow Daily Defense SPF 40
Product NDC 71501-1904
11-digit product format 715011904
Labeler code 71501
Product ID 71501-1904_2de40ee1-ec9e-a4fc-e063-6294a90a7cb1
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE
Dosage form CREAM
Route TOPICAL
Labeler Dr. Loretta, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-02-05
Substance ZINC OXIDE
Active strength 170 mg/mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag No
Listing certified through 2026-12-31
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 Dr Loretta Universal Glow Daily Defense SPF 40
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 170 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 71501-1904-1 Dr Loretta Universal Glow Daily Defense SPF 40 50 mL in 1 TUBE, WITH APPLICATOR CREAM 50 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71501-1904 DR LORETTA UNIVERSAL GLOW DAILY DEFENSE SPF 40 (ZINC OXIDE) CREAM [DR. LORETTA, LLC] 1 Current NDC, 1 package rows 20250221_ebdaf6c1-1572-4840-851b-6d780471fcb2.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 Sample Exclude flag Status 71501-1904-1 71501190401 50 mL in 1 TUBE, WITH APPLICATOR (71501-1904-1) 50 ml 2025-02-05 No No Current