Home NDC 72812-150 Earth Mama Lady Face Mineral Sunscreen - Medium/Dark Tint Broad Spectrum
Product NDC 72812-150
11-digit product format 728120150
Labeler code 72812
Product ID 72812-150_3c30e656-0086-a9fe-e063-6294a90a95bf
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form STICK
Route TOPICAL
Labeler Earth Mama Angel Baby LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-06-05
Substance ZINC OXIDE
Active strength 22 g/100g
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 Earth Mama Lady Face Mineral Sunscreen - Medium/Dark Tint Broad Spectrum
Brand name suffix SPF 40
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 22 g/100g
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# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72812-150-01 Earth Mama Lady Face Mineral Sunscreen - Medium/Dark Tint Broad SpectrumSPF 40 1 in 1 CARTON STICK 1 6 72812-150-01 Earth Mama Lady Face Mineral Sunscreen - Medium/Dark Tint Broad SpectrumSPF 40 21 g in 1 TUBE STICK 21 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72812-150 EARTH MAMA LADY FACE MINERAL SUNSCREEN - MEDIUM/DARK TINT BROAD SPECTRUM SPF 40 (ZINC OXIDE) STICK [EARTH MAMA ANGEL BABY LLC] 4 Current NDC, Legacy NDC, 2 package rows 20240621_908c41fd-0496-4237-813b-1135e10ae0c5.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 72812-150-01 72812015001 1 TUBE in 1 CARTON (72812-150-01) / 21 g in 1 TUBE 1 tube 2020-06-08 2026-12-31 No No Current