SUNZONE FAMILY SUNSCREEN SPF 30
- Product NDC
- 50021-144
- 11-digit product format
- 500210144
- Labeler code
- 50021
- Product ID
- 50021-144_38676290-f5ea-470f-bf1c-7c4fce8b059d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Octocrylene, Octisalate, Oxybenzone, Avobenzone and Homosalate.
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- Empack Spraytech Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2012-11-08
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTOCRYLENE; OCTISALATE; OXYBENZONE; AVOBENZONE; HOMOSALATE
- Active strength
- 11 g/153g; g/153g; g/153g; g/153g; g/153g; g/153g
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#