71609-0009 : Premium Ultra Uv Pure Sun Topical Stick
| NDC: | 71609-0009 |
| Labeler: | Purecell Korea Co., Ltd. |
| Product Type: | Human OTC Drug |
| Drug Name: | Premium Ultra Uv Pure Sun |
| Dosage Form: | Topical Stick |
| Application #: | part352 |
| Rev. Date: |
NDC Package Codes:
- 71609-0009-1: 15 G IN 1 CONTAINER (71609‑0009‑1)
Active Ingredients:
- Octinoxate
- Diethylamino Hydroxybenzoyl Hexyl Benzoate
- Octisalate
- Bemotrizinol
- Octocrylene
Dosage Strength:
- 7 g/100g
- 7 g/100g
- 5 g/100g
- 2 g/100g
- 8 g/100g
NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.
