Home NDC 84763-010 CENTELLA SUNSCREEN Cream
Product NDC 84763-010
11-digit product format 847630010
Labeler code 84763
Product ID 84763-010_4cbac4e9-7541-f703-e063-6394a90ad808
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form CREAM
Route TOPICAL
Labeler Yunqi Cosmetics (Shenzhen) Co., Ltd
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-03-11
Substance ZINC OXIDE
Active strength .24 g/mL
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 CENTELLA SUNSCREEN Cream
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE .24 g/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 84763-010-01 CENTELLA SUNSCREEN Cream 100 mL in 1 BOTTLE CREAM 100 1 84763-010-01 CENTELLA SUNSCREEN Cream 1 in 1 BOX CREAM 1 1
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 109 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 84763-010-01 84763001001 1 BOTTLE in 1 BOX (84763-010-01) / 100 mL in 1 BOTTLE 1 bottle 2026-03-11 No No Current