Home NDC 85163-006 OUHOE Ultra Anti-Acne Control Gel
Product NDC 85163-006
11-digit product format 851630006
Labeler code 85163
Product ID 85163-006_448df74a-3d37-8b21-e063-6294a90af122
Type HUMAN OTC DRUG
Nonproprietary name GLYCERIN
Dosage form GEL
Route TOPICAL
Labeler Shantou Ouhoe Technology Co., Ltd.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-08-08
Substance CERAMIDE NP
Active strength .004 mg/20mg
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 Ultra Anti-Acne Control Gel
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CERAMIDE NP .004 mg/20mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4370DF050B 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 85163-006-01 OUHOE Ultra Anti-Acne Control Gel 20 mg in 1 BOX GEL 20 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 38 of 68 · 1,350 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85163-006-01 85163000601 20 mg in 1 BOX (85163-006-01) 20 mg 2025-08-08 No No Current