VIOFAIRY 5% Minoxidil Spray.

Manufacturer
Shenzhen Shandian Jingling Technology Co., Ltd.
Effective date
2024-01-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:08:07

Label at a glance#

ProductVIOFAIRY 5% Minoxidil Spray.
Active ingredientMINOXIDIL
Label structure14 sections

Dosage and administration

.Apply 1ml(5 Sprays) twice a day. Once in the morning and another time in the evening before bed .Spray directly on top of the scalp in the area to be treated Using more than directed or more often will not improve results . Continued use is necessary to increase and then maintain your hair regrowth . . Discontinuing use may result in hair loss.

Storage and handling

Before use, read all information on the carton Store at controlled room temperature 20 to 25 C (68 to 77°F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Minoxidil 5%

Purpose

OTC - PURPOSE SECTION

Hair Regrowth Treatment

Use

INDICATIONS & USAGE SECTION

to regrow hair on the top of the scalp

Warnings

WARNINGS SECTION

For external use only

Keep away from fire and flam

Do not use

OTC - DO NOT USE SECTION

You have no family history of hair loss,hair loss is sudden and/or patchy

you are under 18 years of age.Do not use it on babies and children

When Using

OTC - WHEN USING SECTION

Do not apply on other parts of the body

void contact with eyes. In case of accidental contact, rinse eyes with a large amount of cool tap water

It takes time to regrow hair. You may need to use this product 2 times a day for a least 4 months before you see results, The amount of hair regrowth is different for each person

Stop Use

OTC - STOP USE SECTION

chest pain, rapid heart beat, faintness, or dizziness occurs

sudden, unexplained weight gain occurs

your hands or feet swell

scalp irritation or redness occurs May be harmful if used when pregnant or breast-feeding
. Keep Out Of Reach Of Children:If swallowed, get medical help or contact a Poison Control Center right away.

Ask Doctor

OTC - ASK DOCTOR SECTION

When Pregnant or breast-feeding

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

DOSAGE & ADMINISTRATION SECTION

.Apply 1ml(5 Sprays) twice a day. Once in the morning and another time in the evening before bed
.Spray directly on top of the scalp in the area to be treated Using more than directed or more often will not improve results
. Continued use is necessary to increase and then maintain your hair regrowth .
. Discontinuing use may result in hair loss.

Other information

STORAGE AND HANDLING SECTION

Before use, read all information on the carton

Store at controlled room temperature 20 to 25 C (68 to 77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

biotin
Deionized Water
Propylene Glycol
Ethyl Alcohol
Potassium Sorbate
GABA

Questions

OTC - QUESTIONS SECTION

service@amazonfairy.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1537948minoxidil 5 % Topical SprayPSN1
1537948minoxidil 50 MG/ML Topical SpraySCD1
1537948minoxidil 5 % Topical SpraySY1

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83804-105-01VIOFAIRY 5% Minoxidil Spray.100 mL in 1 BOTTLELIQUID1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83804-105VIOFAIRY 5% MINOXIDIL SPRAY. (5% MINOXIDIL SPRAY.) LIQUID [SHENZHEN SHANDIAN JINGLING TECHNOLOGY CO., LTD.]11 package rows20240201_103bbd07-1f1c-1d98-e063-6394a90a6ca4.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83804-10583804-105-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
103bbd07-1f1d-1d98-e063-6394a90a6ca4103bbd07-1f1c-1d98-e063-6394a90a6ca42024-01-31WarningsExact identifier
spl id: 103bbd07-1f1d-1d98-e063-6394a90a6ca4
spl set id: 103bbd07-1f1c-1d98-e063-6394a90a6ca4

Reported adverse events (FAERS/openFDA)#

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