JEUNCELL Hair restorer and Hair Growth Solution
- Manufacturer
- Jeun Cell Ltd
- Effective date
- 2012-11-25
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:33:48
Label at a glance#
Label contents#
Full prescribing information#
INACTIVE INGREDIENT SECTION
purified water, coco betaine, cocamidopropyl betaine, decyl polyglucose, black sesame ext, black soybean ext, lycium chinense fruit ext, pine needle ext, chrysanthemum morifolium flower ext, eclipta ext, thuja orientalis leaf ext, dodder ext, strawberry ext, polygonum multiflorim root ext, artemisia vulgaris ext, chungung ext, seaweed ext, laminaria japonica ext, acorus
OTC - PURPOSE SECTION
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
INDICATIONS & USAGE SECTION
■ Use 1-3ml (Shampoo and rinse with 2ml and use the rest 1ml again) two times each one every day.
WARNINGS SECTION
DOSAGE & ADMINISTRATION SECTION
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| NIACIN Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| e2dae634-14ed-febf-08ee-93196433b5b7 | Product name | 9 | 20190614 |
| 0a5e5249-329b-0cff-e714-77159f193a87 | Product name | 1 | 20140508 |
| 6b7a6f32-42a6-994d-5ab6-d180e92ee9d8 | Product name | 1 | 20140508 |
| d394f843-7479-dc48-dbd3-232266c5548c | Product name | 1 | 20140508 |
| dc9a5fb6-14e2-1cc8-a567-a781fd1f0212 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 54296-3001-1 | 2019-11-27 | C162847 | 48780-1 | 9855d018-dfdc-cd31-e053-dbdaa90ab51a | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54296-3001-1 | JEUNCELL Hair restorer and Hair Growth Solution | 300 mL in 1 BOTTLE | SHAMPOO | 300 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 54296-3001 | JEUNCELL HAIR RESTORER AND HAIR GROWTH SOLUTION (NIACIN) SHAMPOO [JEUN CELL LTD] | 1 | Legacy NDC, 1 package rows | 20121127_ef22b808-7bcc-413a-925a-4dc1f70f36a9.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| NIACIN | ACTIVE INGREDIENT | 2679MF687A | 1 | |
| NIACIN | ACTIVE MOIETY | 2679MF687A | 1 | |
| ACORUS CALAMUS ROOT | INACTIVE INGREDIENT | XY1K7KIQ0F | 1 | |
| ARTEMISIA VULGARIS ROOT | INACTIVE INGREDIENT | 32MP823R8S | 1 | |
| ASIAN GINSENG | INACTIVE INGREDIENT | CUQ3A77YXI | 1 | |
| CAPSICUM | INACTIVE INGREDIENT | 00UK7646FG | 1 | |
| CHRYSANTHEMUM X MORIFOLIUM FLOWER | INACTIVE INGREDIENT | 2GR3C1A0WV | 1 | |
| COCAMIDOPROPYL BETAINE | INACTIVE INGREDIENT | 5OCF3O11KX | 1 | |
| DEXPANTHENOL | INACTIVE INGREDIENT | 1O6C93RI7Z | 1 | |
| ECLIPTA PROSTRATA WHOLE | INACTIVE INGREDIENT | 8138AB7E8Y | 1 | |
| FALLOPIA MULTIFLORA ROOT | INACTIVE INGREDIENT | AUZ3VD75MC | 1 | |
| GREEN TEA LEAF | INACTIVE INGREDIENT | W2ZU1RY8B0 | 1 | |
| JOJOBA OIL | INACTIVE INGREDIENT | 724GKU717M | 1 | |
| LAMINARIA JAPONICA | INACTIVE INGREDIENT | WE98HW412B | 1 | |
| LYCIUM CHINENSE FRUIT | INACTIVE INGREDIENT | TG711Q7A1Q | 1 | |
| NORI | INACTIVE INGREDIENT | 477TV3P5UX | 1 | |
| PINE NEEDLE OIL (PINUS MUGO) | INACTIVE INGREDIENT | 6KF1RLN1CI | 1 | |
| PLATYCLADUS ORIENTALIS LEAF | INACTIVE INGREDIENT | 32E5V7G32B | 1 | |
| ROSEMARY | INACTIVE INGREDIENT | IJ67X351P9 | 1 | |
| SESAME OIL | INACTIVE INGREDIENT | QX10HYY4QV | 1 | |
| SODIUM BENZOATE | INACTIVE INGREDIENT | OJ245FE5EU | 1 | |
| STRAWBERRY | INACTIVE INGREDIENT | 4J2TY8Y81V | 1 | |
| TRIPTERYGIUM WILFORDII ROOT | INACTIVE INGREDIENT | 06Q6W5UGMZ | 1 |
Products#
Every source-derived product name is available through these pages.
- JEUNCELL Hair restorer and Hair Growth Solution
- NIACIN
- PINE NEEDLE OIL (PINUS MUGO)
- TRIPTERYGIUM WILFORDII ROOT
- COCAMIDOPROPYL BETAINE
- SESAME OIL
- LYCIUM CHINENSE FRUIT
- CHRYSANTHEMUM X MORIFOLIUM FLOWER
- ECLIPTA PROSTRATA WHOLE
- PLATYCLADUS ORIENTALIS LEAF
- STRAWBERRY
- FALLOPIA MULTIFLORA ROOT
- ARTEMISIA VULGARIS ROOT
- NORI
- LAMINARIA JAPONICA
- ACORUS CALAMUS ROOT
- CAPSICUM
- GREEN TEA LEAF
- ASIAN GINSENG
- JOJOBA OIL
- DEXPANTHENOL
- ROSEMARY
- SODIUM BENZOATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 54296-3001 | 54296-3001-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | INJECTION / INTRAMUSCULAR | 864 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | TABLET, DELAYED RELEASE / ORAL | 0.34 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | POWDER, FOR SOLUTION / ORAL | 98 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | PASTE, DENTIFRICE / DENTAL | 0.5 %w/w | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SPONGE / TOPICAL | NA | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | ENEMA / RECTAL | 60 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | TABLET / ORAL | 30 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | GRANULE, EFFERVESCENT / ORAL | 60 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SUSPENSION/ DROPS / ORAL | 23 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | CREAM / TOPICAL | 0.2 %w/w | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | INJECTION, EMULSION / INTRAVENOUS | 0.1 %w/v | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | GEL / DENTAL | 0.08 %w/w | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | GRANULE / ORAL | NA | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SUSPENSION, EXTENDED RELEASE / ORAL | 24 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | TABLET, EXTENDED RELEASE / ORAL | NA | ||
| STRAWBERRY | STRAWBERRY | 4J2TY8Y81V | SOLUTION / ORAL | 6 mg | ||
| SESAME OIL | SESAME OIL | QX10HYY4QV | CAPSULE / ORAL | 2325 mg | ||
| STRAWBERRY | STRAWBERRY | 4J2TY8Y81V | SYRUP / ORAL | 2.5 mg/5ml | ||
| STRAWBERRY | STRAWBERRY | 4J2TY8Y81V | TABLET, ORALLY DISINTEGRATING / ORAL | 1 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | CONCENTRATE / ORAL | 20 mg | ||
| STRAWBERRY | STRAWBERRY | 4J2TY8Y81V | POWDER, FOR SUSPENSION / ORAL | 20 mg/5ml | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | PASTE / ORAL | 28 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | TABLET, COATED / ORAL | 0.2 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SUSPENSION / ORAL | 320 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | GRANULE, FOR SUSPENSION / ORAL | 120 mg | ||
| SESAME OIL | SESAME OIL | QX10HYY4QV | INJECTION / INTRAMUSCULAR | 70 %v/v | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | POWDER, FOR SUSPENSION / ORAL | 160 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | CAPSULE / ORAL | 8.5 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | GEL / RECTAL | 406 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SYRUP / ORAL | 80 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | INJECTION / INTRAVENOUS | 864 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | ELIXIR / ORAL | 5.02 mg/5ml | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | INJECTION, SOLUTION / INTRAMUSCULAR | 4.8 %w/v | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | GEL / TOPICAL | 5 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | TABLET, FILM COATED / ORAL | 1 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SYSTEM / TOPICAL | 2 mg | ||
| STRAWBERRY | STRAWBERRY | 4J2TY8Y81V | SUSPENSION / ORAL | 21 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | FILM, SOLUBLE / BUCCAL | 3 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SOLUTION / TOPICAL | 0.1 %w/v | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SOLUTION / ORAL | 660 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | FILM / BUCCAL | 1 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | PASTE / DENTAL | 0.08 %w/w |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| b047040a-c85b-4c6a-89f2-09ab994b1785 | ef22b808-7bcc-413a-925a-4dc1f70f36a9 | 2012-11-25 | Warnings | b047040a-c85b-4c6a-89f2-09ab994b1785 ef22b808-7bcc-413a-925a-4dc1f70f36a9 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
