Home NDC 81104-103 COLLAGEN GLOW MINERAL SUNSCREEN
Product NDC 81104-103
11-digit product format 811040103
Labeler code 81104
Product ID 81104-103_383fdc7a-34fe-f118-e063-6394a90acc46
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE
Dosage form LOTION
Route TOPICAL
Labeler NAKED SUNDAYS PTY LTD
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-12-01
Substance ZINC OXIDE
Active strength 22.75 g/100mL
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 COLLAGEN GLOW MINERAL SUNSCREEN
Brand name suffix SPF 50
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 22.75 g/100mL
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 81104-103-11 COLLAGEN GLOW MINERAL SUNSCREENSPF 50 50 mL in 1 TUBE LOTION 50 13 81104-103-12 COLLAGEN GLOW MINERAL SUNSCREENSPF 50 20 mL in 1 TUBE LOTION 20 13 81104-103-13 COLLAGEN GLOW MINERAL SUNSCREENSPF 50 80 mL in 1 TUBE LOTION 80 13
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81104-103 COLLAGEN GLOW MINERAL SUNSCREEN SPF 50 (ZINC OXIDE) LOTION [NAKED SUNDAYS PTY LTD] 11 Current NDC, Legacy NDC, 3 package rows 20250402_f76a4f0d-e3a6-4bd4-b1ab-09d690976d96.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 81104-103-11 81104010311 50 mL in 1 TUBE (81104-103-11) 50 ml 2020-12-01 0000-00-00 No No Current 81104-103-12 81104010312 20 mL in 1 TUBE (81104-103-12) 20 ml 2020-12-01 0000-00-00 No No Current 81104-103-13 81104010313 80 mL in 1 TUBE (81104-103-13) 80 ml 2020-12-01 No No Current