Home NDC 85212-0006 QIDILA Whitening Skin Lightening Cream
Product NDC 85212-0006
11-digit product format 852120006
Labeler code 85212
Product ID 85212-0006_2e66a508-3f57-4500-e063-6394a90aaa9d
Type HUMAN OTC DRUG
Nonproprietary name BUTYLENE GLYCOL,BUTYROSPERMUM PARKII (SHEA BUTTER),KYOUNIN YU,TOCOPHEROL,ASCORBIC ACID,NIACINAMIDE
Dosage form CREAM
Route EXTRACORPOREAL
Labeler Beijing JUNGE Technology Co., Ltd.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-01
Substance ASCORBIC ACID; BUTYLENE GLYCOL; BUTYROSPERMUM PARKII (SHEA) BUTTER; NIACINAMIDE; PRUNUS ARMENIACA (APRICOT) KERNEL EXTRACT; TOCOPHEROL
Active strength .05; 5; 3; .05; 2; 1 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
Pharmacologic classes Ascorbic Acid [CS], Vitamin C [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base QIDILA Whitening Skin Lightening Cream
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TOCOPHEROL .05 g/100mL BUTYROSPERMUM PARKII (SHEA) BUTTER 5 g/100mL PRUNUS ARMENIACA (APRICOT) KERNEL EXTRACT 3 g/100mL NIACINAMIDE .05 g/100mL BUTYLENE GLYCOL 2 g/100mL ASCORBIC ACID 1 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 6 matching rows.
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 85212-0006-1 QIDILA Whitening Skin Lightening Cream 30 mL in 1 BOTTLE CREAM 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 85212-0006 QIDILA WHITENING SKIN LIGHTENING CREAM (BUTYLENE GLYCOL,BUTYROSPERMUM PARKII (SHEA BUTTER),KYOUNIN YU,TOCOPHEROL,ASCORBIC ACID,NIACINAMIDE) CREAM [BEIJING JUNGE TECHNOLOGY CO., LTD.] 1 Current NDC, 1 package rows 20250221_2e66a508-3f56-4500-e063-6394a90aaa9d.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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85212-0006-1 85212000601 30 mL in 1 BOTTLE (85212-0006-1) 30 ml 2025-01-01 No No Current