The21 DAYs HAIR NUTRIENT SERUM

Manufacturer
GDKCOSMETICS Co., Ltd
Effective date
2014-01-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:37:45

Label at a glance#

ProductThe21 DAYs HAIR NUTRIENT SERUM
Active ingredientGlycerin
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

glycerin


INACTIVE INGREDIENT SECTION

water, aloe barbadensis leaf juice, butylene glycol, alcohol, liminaria japonica ext, sodium hyaluronate, spirulina platensis powder, hydroxyethycellulose, carbomer, sorbitan sesquioleate, triethanolamine, swerita japonica ext, citric acid, panthenol, niacinamide, peg-60 hydrogenated castor oil, jojoba seed ext, hippophae rhamnoidese ext, walnut seed ext, avocado fruit ext, matricaria flower ext, nettle ext, sambucus nigra fruit ext, chrysanthemum morifolium flower ext, vitextrifolia fruit ext, thuja occidentalis leaf ext, cnidium officinale foot ext, angelica dahurica root ext, asarum sieboldi root ext, morus alba root ext, eclipta prostrata ext, asrum sieboldi root ext, morus alba root ext, eclipta prostrata ext, phenoxyethanol, methylparaben, ethylparaben, butylparaben, propylparaben, isobutylparaben, polygonium multiflorum root ext, soybean seed ext, lysine hcl, proline, sodium ascorbyl phosphate, acetyl methionine, theanine, biotim fragrance, copper tripeptide-1, rh-olipeptide-1, panax ginseng callus culture ext, colloidal platinum, hydrolyzed pea protein, lecithin, olive fruit oil, phytosterols, squalane, shea butter, ceramide 3, propanediol


OTC - PURPOSE SECTION

to promote healthy hair and provides nutritional support for the scalp and hair follicles


OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children


INDICATIONS & USAGE SECTION

apply two times a day in the morning and evening, massage into your balding and thinning areas


WARNINGS SECTION

- avoid using on blemishes, pimples, irritated or sunburned skin
- discontinue use if irritation develops or increases


DOSAGE & ADMINISTRATION SECTION

for dental use only


PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label
package label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809115029959GTIN-13: 8809115029959
EAN-13: 8809115029959
GTIN storage (14 digits): 08809115029959
label.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60614-1001-22019-11-27C16284748780-19855e2a2-4d58-60a7-e053-dbdaa90a05bdDrug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
GlycerinACTIVE INGREDIENTPDC6A3C0OX2
GlycerinACTIVE MOIETYPDC6A3C0OX2
BUTYLENE GLYCOLINACTIVE INGREDIENT3XUS85K0RA2
CARBAMIDE PEROXIDEINACTIVE INGREDIENT31PZ2VAU812
HYALURONATE SODIUMINACTIVE INGREDIENTYSE9PPT4TH2
PANTHENOLINACTIVE INGREDIENTWV9CM0O67Z2
SORBITAN SESQUIOLEATEINACTIVE INGREDIENT0W8RRI5W5A2
WATERINACTIVE INGREDIENT059QF0KO0R2

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
60614-100160614-1001-1, 60614-1001-2

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

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 · 9 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
HYALURONATE SODIUMHYALURONATE SODIUMYSE9PPT4THINJECTION, SUSPENSION / INTRAMUSCULAR23 mgExact identifier — unii candidate
5 equally ranked IID candidates
SORBITAN SESQUIOLEATESORBITAN SESQUIOLEATE0W8RRI5W5AOINTMENT / RECTAL15 mgExact identifier — unii candidate
2 equally ranked IID candidates
HYALURONATE SODIUMHYALURONATE SODIUMYSE9PPT4THLOTION / TOPICAL0.01 %w/wExact identifier — unii candidate
5 equally ranked IID candidates
SORBITAN SESQUIOLEATESORBITAN SESQUIOLEATE0W8RRI5W5AOINTMENT / TOPICAL75 mgExact identifier — unii candidate
2 equally ranked IID candidates
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
2 equally ranked IID candidates
HYALURONATE SODIUMHYALURONATE SODIUMYSE9PPT4THGEL / TOPICAL463 mgExact identifier — unii candidate
5 equally ranked IID candidates
HYALURONATE SODIUMHYALURONATE SODIUMYSE9PPT4THINJECTION, SUSPENSION / INTRA-ARTICULAR23 mgExact identifier — unii candidate
5 equally ranked IID candidates
HYALURONATE SODIUMHYALURONATE SODIUMYSE9PPT4THINJECTION, SUSPENSION / INTRAVITREAL23 mgExact identifier — unii candidate
5 equally ranked IID candidates
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 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
4d67cc93-2c3d-4a4b-bfbc-48a572d6b37d2801f2ae-96e6-49aa-9b23-62d8dff044852014-01-03WarningsExact identifier
spl id: 4d67cc93-2c3d-4a4b-bfbc-48a572d6b37d
spl set id: 2801f2ae-96e6-49aa-9b23-62d8dff04485

Reported adverse events (FAERS/openFDA)#

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