Sunscreen
- Product NDC
- 55319-788
- 11-digit product format
- 553190788
- Labeler code
- 55319
- Product ID
- 55319-788_6133dc7d-72a8-4c04-bae3-33039923be3e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Family Dollar Services, Inc
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-08-07
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
- Active strength
- 27 mg/g; mg/g; mg/g; mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55319-788-30 | 55319078830 | 170 g in 1 BOTTLE, SPRAY (55319-788-30) | 170 g | 2017-08-07 | 0000-00-00 | No | No | Current |