FDA.reportPublic FDA data

Super vitamin C serum

Manufacturer
FlexiGo Inc
Effective date
2025-09-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:14:14

Label at a glance#

ProductMINOXIDIL
Active ingredientMINOXIDIL
Label structure12 sections

Label contents#

Full prescribing information#

For external use only.When using this product, avoidgetting into eyes. lf contact occurs, rinse thoroughlywith water. lfskin irritation occurs, wash product offand consult a physician.When first applying thisproduct,you may experience a slight tingling sens...

OTC - DO NOT USE SECTION

OTC-DO NOT USE SECTIONOTC-DO NOT USE SECTION

Avoid contact with eyes. lf the product gets into the eye,flush with water for 15 minutes. Avoid inhaling vapors. Cap the bottle tightly. Out of direct sunlight and store at room temperature away from heat.

OTC - WHEN USING SECTION

OTC-WHEN USING SECTIONOTC-WHEN USING SECTION

You become pregnant, or are planning to become pregnant, while using the product. If discomfort persists.

OTC - STOP USE SECTION

OTC-STOP USE SECTIONOTC-STOP USE SECTION

If swallowed, get medical help or contact Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC-KEEP OUT OF REACH OF CHILDREN SECTIONOTC-KEEP OUT OF REACH OF CHILDREN SECTION

Store in a cool, shaded place away from directsunlight. Store at room temperature between15-30°C(59-86°F)

STORAGE AND HANDLING SECTION

STORAGE AND HANDLING SECTIONSTORAGE AND HANDLING SECTION

OTC - ACTIVE INGREDIENT SECTION

OTC-Active IngredientOTC-Active Ingredient

For external use only.

WARNINGS SECTION

WARNINGSWARNINGS

DOSAGE & ADMINISTRATION SECTION

DIRECTIONSDIRECTIONS

INACTIVE INGREDIENT SECTION

Inactive ingredient sectionInactive ingredient section

INDICATIONS & USAGE SECTION

INDICATIONS & USAGE SECTIONINDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

OTC-PURPOSE SECTIONOTC-PURPOSE SECTION

For external use only.When using this product, avoidgetting into eyes. lf contact occurs, rinse thoroughlywith water. lfskin irritation occurs, wash product offand consult a physician.When first applying thisproduct,you may experience a slight tingling sens...

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label.PRINCIPAL DISPLAY PANELpackage label.PRINCIPAL DISPLAY PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1537948minoxidil 5 % Topical SprayPSN3
1537948minoxidil 50 MG/ML Topical SpraySCD3
1537948minoxidil 5 % Topical SpraySY3

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
MINOXIDIL Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85524-2501-1MINOXIDIL1 in 1 BOXLIQUID13
85524-2501-9MINOXIDIL60 mL in 1 BOTTLELIQUID603

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85524-250185524-2501-9, 85524-2501-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
CASTOR OILD5340Y2I9GIACT
PEG-40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
XANTHAN GUMTTV12P4NEEIACT
GLYCERINPDC6A3C0OXIACT
ROSEMARY OIL8LGU7VM393IACT
PANAX NOTOGINSENG ROOTGQX1C1175UIACT
MINOXIDIL5965120SH1ACTIB

Source Document#

Source XML

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
3f0b6642-d1f7-c72a-e063-6394a90a5f9933860fde-8f9e-8fbb-e063-6294a90aae4a2025-09-17WarningsExact identifier
spl id: 3f0b6642-d1f7-c72a-e063-6394a90a5f99
spl set id: 33860fde-8f9e-8fbb-e063-6294a90aae4a

Reported adverse events (FAERS/openFDA)#

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