FDA.reportPublic FDA data

QIDILA 5% Minoxidil Foam

Product NDC
85212-0002
11-digit product format
852120002
Labeler code
85212
Product ID
85212-0002_2d751520-9244-4902-e063-6394a90a374a
Type
HUMAN OTC DRUG
Nonproprietary name
Minoxidil,Biotin
Dosage form
AEROSOL, FOAM
Route
EXTRACORPOREAL
Labeler
Beijing JUNGE Technology Co., Ltd.
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-09-01
Substance
BIOTIN; MINOXIDIL
Active strength
5; 5 g/100mL; g/100mL
Pharmacologic classes
Arteriolar Vasodilation [PE], Arteriolar Vasodilator [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 5% Minoxidil Foam
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MINOXIDIL5 g/100mL
BIOTIN5 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
5965120SH1Internal UNII lookup
6SO6U10H04Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2704021Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2d751520-9243-4902-e063-6394a90a374aAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85212-0002-1QIDILA 5% Minoxidil Foam60 mL in 1 BOTTLEAEROSOL, FOAM601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85212-0002QIDILA 5% MINOXIDIL FOAM (MINOXIDIL,BIOTIN) AEROSOL, FOAM [BEIJING JUNGE TECHNOLOGY CO., LTD.]1Current NDC, 1 package rows20250212_2d751520-9243-4902-e063-6394a90a374a.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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
QIDILA 5% Minoxidil FoamMINOXIDIL,BIOTINBeijing JUNGE Technology Co., Ltd.2d751520-9243-4902-e063-6394a90a374a2025-02-06WarningsExact identifier
ndc (product): 85212-0002

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2704021biotin 5 % / minoxidil 5 % Topical FoamPSN2d751520-9243-4902-e063-6394a90a374a1
2704021biotin 50 MG/ML / minoxidil 50 MG/ML Topical FoamSCD2d751520-9243-4902-e063-6394a90a374a1
2704021biotin 5 % / minoxidil 5 % Topical FoamSY2d751520-9243-4902-e063-6394a90a374a1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85212-0002-18521200020160 mL in 1 BOTTLE (85212-0002-1) 60 ml2024-09-01NoNoCurrent