LumaSilk Emulsion Level 02
- Product NDC
- 71393-005
- 11-digit product format
- 713930005
- Labeler code
- 71393
- Product ID
- 71393-005_51c7d6d4-3652-0a53-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- LumaSilk Emulsion Level 02
- Dosage form
- EMULSION
- Route
- TOPICAL
- Labeler
- The Skin Atelier, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2017-07-01
- Marketing end
- 0000-00-00
- Substance
- HYDROQUINONE
- Active strength
- 0 g/g
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record