OTC - ACTIVE INGREDIENT SECTION
Centella Asiatica Extract
Centella Asiatica Extract
Sodium Hyaluronate, Hamamelis Virginiana (Witch Hazel) Leaf Extract, etc.
Water-soluble massage gel
keep out or reach of the children
With clean hands, dispense an appropriate amount and apply on skin, massaging gently
Precautions for Use
If any of the following conditions occur, discontinue use immediately and consult a dermatologist. Continuous use will cause symptoms to worsen.
1) In case of skin reaction such as red spots, swelling, itch or irritation etc. during use
2) In case of the above skin reaction when applied area is exposed to direct sunlight
Do not use on damaged skin area such as wound, rash or skin infection
Storage and Handling
1) Close lid tightly after use
2) Keep out of reach of infants and children
3) Store in a cool, dry place away from direct sunlight
4) Avoid eye area
for external use only
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 72072-0001-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-188a-f424-e053-dadaa90a57ce | 641fbbe5-dd60-31e2-e053-2991aa0af804 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72072-0001-1 | SHYNOMORE LUBRICANT | 100 mL in 1 TUBE | GEL | 100 | 1 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 72072-0001 | SHYNOMORE LUBRICANT (CENTELLA ASIATICA EXTRACT) GEL [BLUETTE CO., LTD.] | 1 | Legacy NDC, 1 package rows | 20180201_641fbbe5-dd60-31e2-e053-2991aa0af804.zip |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 72072-0001 | 72072-0001-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| HAMAMELIS VIRGINIANA LEAF | T07U1161SV | IACT |
| CENTELLA ASIATICA | 7M867G6T1U | ACTIB |
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 |
|---|---|---|---|---|---|---|
| 641fbbe5-dd67-31e2-e053-2991aa0af804 | 641fbbe5-dd60-31e2-e053-2991aa0af804 | 2018-02-01 | Warnings | 641fbbe5-dd67-31e2-e053-2991aa0af804 641fbbe5-dd60-31e2-e053-2991aa0af804 |
Adverse event summaries are temporarily unavailable. Other product information remains available.