Hair Groth Essence

Manufacturer
Yiwu Ziqiu Import Export Co Ltd
Effective date
2024-11-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:34:27

Label at a glance#

ProductHair Groth Essence
Active ingredientMINOXIDIL
Label structure10 sections

Label contents#

Full prescribing information#

COMPONENTS

Salicylic acid 2%

OTC - PURPOSE SECTION

wart remover

WARNINGS SECTION

Forevemaluseony Avoid coniac wth eves li coniac ocus nse ihorouthly wt waier Keep out ofreach oi chidrenifvou ale preanant.nursing. otiaveanyunderving medca condion.consutyou healthcare provider before using the product

DOSAGE & ADMINISTRATION SECTION

For external use only

OTC - DO NOT USE SECTION

Discontinue use if any irritation or adverse reaction occurs

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes. lf contact occurs, rinse thoroughly with waterDiscontinue use if any irritation or adverse reaction occurs.

OTC - STOP USE SECTION

on broken or irritated scalp

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If sxralowed, get medical help or contact a Poison Conirol Cenler ngiht away.

INACTIVE INGREDIENT SECTION

Acrylates copolymer, Ethyl acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84827-432-012024-12-23C16284748780-129f41ae9-360a-13f5-e063-dbdaa90ac524263bc92a-5bfe-a08f-e063-6294a90a70ae

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84827-432-01Hair Groth Essence5 mL in 1 BOXLIQUID51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84827-432HAIR GROTH ESSENCE LIQUID [YIWU ZIQIU IMPORT EXPORT CO LTD]11 package rows20241107_263bc92a-5bfe-a08f-e063-6294a90a70ae.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84827-43284827-432-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
263bc92a-5bff-a08f-e063-6294a90a70ae263bc92a-5bfe-a08f-e063-6294a90a70ae2024-11-06WarningsExact identifier
spl id: 263bc92a-5bff-a08f-e063-6294a90a70ae
spl set id: 263bc92a-5bfe-a08f-e063-6294a90a70ae

Reported adverse events (FAERS/openFDA)#

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