NDC 62032-116
NU-DERM SUNFADERSkin Lightener with Sunscreen (SPF 15) PABA FREE 40 mg per 1 g / 55 mg per 1 g / 75 mg per 1 g lotion
On the label: Omp, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| G.s. Cosmeceutical Usa, Inc. | Livermore, CA, United States | Makes it | Problems found, fixed voluntarilyAug 14, 2019 · 6 inspections, 1 with FDA action |
Product details
- Generic drug
- Hydroquinone and Octinoxate and Oxybenzone: every company that makes it
- Form
- lotion, topical
- Strength
- 40 mg per 1 g / 55 mg per 1 g / 75 mg per 1 g
- Approval
- UNAPPROVED DRUG OTHER
- On the market since
- Jan 1, 1984
- Package NDCs
62032-116-36- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2025
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