Paulas Choice Lipscreen SPF 50
- Product NDC
- 76144-256
- Requested package NDC
- 76144-256-00
- 11-digit product format
- 761440256
- Labeler code
- 76144
- Product ID
- 76144-256_f08aafdd-19dd-c646-e053-2a95a90af0fc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Homosalate, Octisalate, Avobenzone, Octocrylene
- Dosage form
- LIPSTICK
- Route
- TOPICAL
- Labeler
- Paula's Choice
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2014-10-03
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 30 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76144-256-00 | 76144025600 | 4.15393 mL in 1 TUBE (76144-256-00) | 4.15393 ml | 2014-10-03 | 0000-00-00 | No | No | Current |