LumaSilk Emulsion Level 03
- Product NDC
- 71393-006
- 11-digit product format
- 713930006
- Labeler code
- 71393
- Product ID
- 71393-006_51ca5b57-f48c-716d-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LumaSilk Emulsion Level 03
- 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
- Pharmacologic classes
- Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA],Depigmenting Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record