Sunscreen
- Product NDC
- 55319-752
- 11-digit product format
- 553190752
- Labeler code
- 55319
- Product ID
- 55319-752_38351aeb-43be-4abe-9bff-1fb4117d2439
- 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
- 31 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 |
|---|
| 55319-752-21 | 55319075221 | 89 g in 1 BOTTLE, PLASTIC (55319-752-21) | 89 g | 2017-08-07 | 0000-00-00 | No | No | Current |
| 55319-752-34 | 55319075234 | 236 g in 1 BOTTLE, PLASTIC (55319-752-34) | 236 g | 2017-08-07 | 0000-00-00 | No | No | Current |