Home NDC 73572-012 Personalized Moisturizer SPF 30
Product NDC 73572-012
11-digit product format 735720012
Labeler code 73572
Product ID 73572-012_4573789e-f616-63f7-e063-6294a90a03d1
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide 10.00%
Dosage form LOTION
Route TOPICAL
Labeler Proven Skincare
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-12-08
Substance ZINC OXIDE
Active strength 10 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 Personalized Moisturizer SPF 30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 10 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 73572-012-01 Personalized Moisturizer SPF 30 30 mL in 1 PACKAGE LOTION 30 2
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 73572-012-01 73572001201 30 mL in 1 PACKAGE (73572-012-01) 30 ml 2025-12-08 No No Current