Indications and uses
Indications and usage: After basic skin care, apply adequate amount following the skin texture and gently tap to enhance absorption.
VASHTI
- Manufacturer
- LEADER GREEN CO., LTD.
- Effective date
- 2013-08-30
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:38:07
Label at a glance#
ProductVASHTI
Active ingredientAllantoin
Label structure8 sections
Dosage and administration
Dosage and administration: Take an adequate amount of this product.
Label contents#
Full prescribing information#
ACTIVE INGREDIENT
Active ingredient: Allantoin 0.5%
INACTIVE INGREDIENT
Inactive ingredients: PONCIRUS TRIFOLIATA FRUIT, NARINGINASE, LOBELIA SPICATA LEAF, MINERAL OIL, VITAMINE C
Purpose
Purpose: Skin Protectant
WARNINGS
Warnings:
1. In case of having following symptoms after using this, you're advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist.
1) In case of having problems such as red rash, swollenness, itching, stimulation during usage.
2) In case of having the same symptoms above on the part you put this product on by direct sunlight.
2. You are banned to use it on the part where you have a scar, eczema, or dermatitis.
3. In case of getting it into your eyes, you have to wash it immediately.
KEEP OUT OF REACH OF CHILDREN
Keep out of reach of children:
Keep out of reach of babies and children
Indications and usage
Indications and usage:
After basic skin care, apply adequate amount following the skin texture and gently tap to enhance absorption.
Dosage and administration
Dosage and administration:
Take an adequate amount of this product.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 61221-020-01 | 2019-11-27 | C162847 | 48780-1 | 9855e2a2-4cb9-60a7-e053-dbdaa90a05bd | 7e59b578-161b-458e-953f-ee1da7d456e5 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 61221-020-01 | VASHTI | 50 mL in 1 CARTON | CREAM | 50 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Allantoin | ACTIVE INGREDIENT | 344S277G0Z | 1 | |
| ALLANTOIN | ACTIVE MOIETY | 344S277G0Z | 1 | |
| LOBELIA SPICATA LEAF | INACTIVE INGREDIENT | 1G4GK01F67 | 1 |
Products#
Every source-derived product name is available through these pages.
- VASHTI
- Allantoin
- LOBELIA SPICATA LEAF
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 61221-020 | 61221-020-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Allantoin | 344S277G0Z | ACTIB |
| LOBELIA SPICATA LEAF | 1G4GK01F67 | IACT |
Source Document#
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 |
|---|---|---|---|---|---|---|
| 5a5626dc-ff5a-453b-a928-c199cb0aee4b | 7e59b578-161b-458e-953f-ee1da7d456e5 | 2013-08-30 | Warnings | 5a5626dc-ff5a-453b-a928-c199cb0aee4b 7e59b578-161b-458e-953f-ee1da7d456e5 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.