Kiehls Since 1851 Activated Sun Protector For Body Broad Spectrum SPF 50 Sunscreen
- Product NDC
- 49967-078
- 11-digit product format
- 499670078
- Labeler code
- 49967
- Product ID
- 49967-078_85355c71-cefb-45b4-a82b-70445e06af89
- 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
- 2012-05-01
- 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
- 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 |
|---|
| 49967-078-01 | 49967007801 | 150 mL in 1 BOTTLE (49967-078-01) | 150 ml | 2012-05-01 | 0000-00-00 | No | No | Current |