Home NDC 85163-016 OUHOE Universal Colored Moisturizer
Product NDC 85163-016
11-digit product format 851630016
Labeler code 85163
Product ID 85163-016_4634fdcd-6f0f-25ca-e063-6294a90a196e
Type HUMAN OTC DRUG
Nonproprietary name TITANIUM DIOXIDE
Dosage form CREAM
Route TOPICAL
Labeler Shantou Ouhoe Technology Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-12-18
Substance CENTELLA ASIATICA
Active strength .01 mg/50mg
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 OUHOE Universal Colored Moisturizer
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CENTELLA ASIATICA .01 mg/50mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 7M867G6T1U Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85163-016-01 OUHOE Universal Colored Moisturizer 50 mg in 1 BOTTLE, PLASTIC CREAM 50 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 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 85163-016-01 85163001601 50 mg in 1 BOTTLE, PLASTIC (85163-016-01) 50 mg 2025-12-18 No No Current