Carenice 5% Minoxidil HAIR REGROWTH TREATMENT

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Carenice 5% Minoxidil HAIR REGROWTH TREATMENT
Generic name: MINOXIDIL 5%
Manufacturer: Shenzhen Yifusi Technology Co., Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: 3e4254d1-a0ce-a347-e063-6294a90a9d92
SPL ID: 3e4254d1-a0cf-a347-e063-6294a90a9d92
Version: 1
Effective date: 2025-09-07
Source export date: 2026-11-06
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:52:36

Harmonized routes table
Harmonized routes
TOPICAL

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Carenice 5% Minoxidil HAIR REGROWTH TREATMENT	openfda.brand_name
generic name		MINOXIDIL 5%	openfda.generic_name
manufacturer name		Shenzhen Yifusi Technology Co., Ltd.	openfda.manufacturer_name
ndc	package	87086-001-02	openfda.package_ndc
ndc	package	87086-001-03	openfda.package_ndc
ndc	package	87086-001-01	openfda.package_ndc
ndc	package	87086-001-05	openfda.package_ndc
ndc	package	87086-001-04	openfda.package_ndc
ndc	product	87086-001	openfda.product_ndc
ndc11	package	87086000102	derived:openfda.package_ndc
ndc11	package	87086000104	derived:openfda.package_ndc
ndc11	package	87086000101	derived:openfda.package_ndc
ndc11	package	87086000105	derived:openfda.package_ndc
ndc11	package	87086000103	derived:openfda.package_ndc
rxcui		645146	openfda.rxcui
spl id		3e4254d1-a0cf-a347-e063-6294a90a9d92	id
spl set id		3e4254d1-a0ce-a347-e063-6294a90a9d92	set_id
unii		5965120SH1	openfda.unii

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

For external use only For use by men only Extremely Flammable:Avoid fire,flame,or smoking during and immediately following application.

Adverse event summaries are temporarily unavailable. Other product information remains available.