La Roche Posay Laboratoire Dermatologique Anthelios 45 Ultra Light Sunscreen Fluid Water Resistant 40
- Product NDC
- 49967-222
- 11-digit product format
- 499670222
- Labeler code
- 49967
- Product ID
- 49967-222_a5b1ba1d-8a18-4766-9243-e4a055198212
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, Octocrylene and Oxybenzone
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- L'Oreal USA Products Inc
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2010-04-01
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
- Active strength
- 30 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 49967-222-01 | 49967022201 | 1 BOTTLE in 1 CARTON (49967-222-01) > 50 mL in 1 BOTTLE | 1 bottle | 2010-04-01 | 0000-00-00 | No | No | Current |