Indications and uses
Uses: The Needle Puff containing Nepidermin (DW-EGF™) helps to deliver nutrients to the skin efficiently.
Uses: The Needle Puff containing Nepidermin (DW-EGF™) helps to deliver nutrients to the skin efficiently.
Directions: Combine sterilized Derma Needle 3000 Shot with the Derma Needle 3000 Shot Roller. Apply half of the Derma Oneshot Ampoule on the face and proceed with massaging thoroughly(5~10 minutes). Apply the rest of the ampoule on the face and remove Derma Needle 3000 Shot and dispose after done using.
Active ingredients: Nepidermin 0.0001 % (1ppm)
Inactive ingredients:
Sodium hyaluronate, Algin, Lactose, Glycerin, Simmondsia Chinensis(jojoba) See Oil, Propanediol, Caprylyl Glycol, Madecassoside, Ethylhexyglycerin, Acetyl hexapeptide-8
Purpose: Wrinkle improvement
Warnings:
For external use only. Keep out of reach of children. Do not use in wounds, eczemas or dermatitis. If you develop rash, itchiness or irritation, discontinue the use. Keep in a cool and dry place. Do not give strong impacts or drop the product. Use immediately after opening and do not re-use the Needle since it is a disposable product.
KEEP OUT OF REACH OF CHILDREN
Uses:
The Needle Puff containing Nepidermin (DW-EGF™) helps to deliver nutrients to the skin efficiently.
Directions:
Combine sterilized Derma Needle 3000 Shot with the Derma Needle 3000 Shot Roller. Apply half of the Derma Oneshot Ampoule on the face and proceed with massaging thoroughly(5~10 minutes). Apply the rest of the ampoule on the face and remove Derma Needle 3000 Shot and dispose after done using.
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 60565-260 | 60565-260-01, 60565-260-02 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Nepidermin | TZK30RF92W | ACTIB |
| Glycerin | PDC6A3C0OX | IACT |
| Propanediol | 5965N8W85T | IACT |
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 |
|---|---|---|---|---|---|---|
| b6d503a3-90c9-488b-b08a-e1a4271c8aaf | 5322ffb2-5236-4e59-ad56-33892c10b10c | 2022-11-10 | Warnings | 5322ffb2-5236-4e59-ad56-33892c10b10c |
Adverse event summaries are temporarily unavailable. Other product information remains available.