FDA.reportPublic FDA data

JINHANCHO

Manufacturer
The Anna | Enveco Cosmetic Co., Ltd.
Effective date
2014-10-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:34:45

Label at a glance#

ProductJINHANCHO
Active ingredientSALICYLIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

salicylic acid


INACTIVE INGREDIENT SECTION

Water■Sodium Laureth Sulfate■Sodium Lauryl Sulfate■Cocamidopropyl Betaine■Cetearyl Alcohol■Nicotinic acid amide■Sodium Chloride■Cocamide DEA■Glycol Distearate■Methylparaben■Caramel Color■perfume■Polygonum Multiflorum Root Extract 
■Glycyrrhiza Glabra (Licorice) Root Extract ■Sophora Angustifolia Root Extract■Camellia Sinensis Leaf Extract■Morus Alba Bark Extract■Aloe Barbadensis Leaf Extract■Coix Lacryma-Jobi Ma-yuen Seed Extract■Acorus Calamus Root Extract Citric Acid■Disodium EDTA■Methylchloroisothiazolinone


OTC - PURPOSE SECTION

hair loss prevention and hair grower


OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out or reach of the children


INDICATIONS & USAGE SECTION

■Apply only scalp
■Apply over twice a day and always after wash your hair
■Apply sufficient quantity to intended part
■Shake well before use



WARNINGS SECTION

For external use only, Do not swallow
When using this product
■keep out of eyes, ears, and mouth. If contact occurs, rinse with plenty of worm or cold water right away and in a serious situation, contact a physician. If swallowing, drink plenty of water and contact a physician



DOSAGE & ADMINISTRATION SECTION

for exernal use only


PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label
package label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69294-1001-12026-01-05C16284748780-19d75b9d0-398b-f424-e053-dadaa90a57ceDrug Facts
69294-1001-12020-01-31C16284748780-19d75b9d0-398b-f424-e053-dadaa90a57ceDrug Facts

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69294-1001JINHANCHO (SALICYLIC ACID) SHAMPOO [THE ANNA]1Legacy NDC20141023_b414b86c-4695-4468-9fa2-620c6cdefe0e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SALICYLIC ACIDACTIVE INGREDIENTO414PZ4LPZ1
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ1
SODIUM LAURETH SULFATEINACTIVE INGREDIENTBPV390UAP01
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69294-100169294-1001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 5 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
SODIUM LAURETH SULFATESODIUM LAURETH-3 SULFATEBPV390UAP0CREAM / TOPICALNAExact identifier — unii candidate
5 equally ranked IID candidates
SODIUM LAURETH SULFATESODIUM LAURETH-3 SULFATEBPV390UAP0SHAMPOO / TOPICAL3192 mgExact identifier — unii candidate
5 equally ranked IID candidates
SODIUM LAURETH SULFATESODIUM LAURETH-3 SULFATEBPV390UAP0SPRAY / TOPICAL0.1 %w/wExact identifier — unii candidate
5 equally ranked IID candidates
SODIUM LAURETH SULFATESODIUM LAURETH-3 SULFATEBPV390UAP0TABLET / ORAL0.91 mgExact identifier — unii candidate
5 equally ranked IID candidates
SODIUM LAURETH SULFATESODIUM LAURETH-3 SULFATEBPV390UAP0CAPSULE / ORAL3.5 mgExact identifier — unii candidate
5 equally ranked IID candidates

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
479f3e6e-df75-53d2-e063-6394a90a75efb414b86c-4695-4468-9fa2-620c6cdefe0e2026-01-05WarningsExact identifier
spl set id: b414b86c-4695-4468-9fa2-620c6cdefe0e

Reported adverse events (FAERS/openFDA)#

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