Skinprint Ultra Sheer SPF 20
- Product NDC
- 71393-012
- 11-digit product format
- 713930012
- Labeler code
- 71393
- Product ID
- 71393-012_5f0df3d2-dc93-1113-e053-2991aa0a2b7d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Skinprint Ultra Sheer SPF 20
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- The Skin Atelier, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2010-10-06
- Marketing end
- 0000-00-00
- Substance
- HOMOSALATE; OXYBENZONE; OCTISALATE; ENSULIZOLE; OCTOCRYLENE; AVOBENZONE
- Active strength
- 15 g/100g; g/100g; g/100g; g/100g; g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record