Home NDC 85212-0040 YVTYVT DARK SPOT
Product NDC 85212-0040
11-digit product format 852120040
Labeler code 85212
Product ID 85212-0040_352699fa-f747-c931-e063-6394a90a6391
Type HUMAN OTC DRUG
Nonproprietary name DARK SPOT
Dosage form LOTION
Route EXTRACORPOREAL
Labeler Beijing JUNGE Technology Co., Ltd.
Application ANDA075357
Marketing category ANDA
Marketing start 2025-01-01
Substance ASCORBIC ACID; KOJIC ACID
Active strength 2; 1 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 Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 2 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A075357-001 MINOXIDIL (FOR MEN) MINOXIDIL 2% SOLUTION / TOPICAL 1999-07-30 A075357-002 MINOXIDIL (FOR WOMEN) MINOXIDIL 2% SOLUTION / TOPICAL 1999-07-30
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-08-01 22:54:32 2026-06 A075357-001 MINOXIDIL (FOR MEN) 2% SOLUTION / TOPICAL 1999-07-30 a50c72e98297…2026-08-01 22:54:32 2026-06 A075357-002 MINOXIDIL (FOR WOMEN) 2% SOLUTION / TOPICAL 1999-07-30 a50c72e98297…
openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 18 matching rows.
Additional Listing Data#
Finished product Yes
Brand name base YVTYVT DARK SPOT
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength KOJIC ACID 2 g/100mL ASCORBIC ACID 1 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 6K23F1TT52 Internal UNII lookup PQ6CK8PD0R 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 85212-0040-1 YVTYVT DARK SPOT 1 mL in 1 BOX LOTION 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 85212-0040 YVTYVT DARK SPOT (DARK SPOT) LOTION [BEIJING JUNGE TECHNOLOGY CO., LTD.] 1 Current NDC, 1 package rows 20250516_352699fa-f746-c931-e063-6394a90a6391.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85212-0040-1 85212004001 1 mL in 1 BOX (85212-0040-1) 1 ml 2025-01-01 No No Current