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LOreal Paris Sublime Sun
LOreal Paris Sublime Sun - 49967-371-01 - (Avobenzone Homosalate Octisalate Octocrylene Oxybenzone)
Drug Information of LOreal Paris Sublime Sun
| Product NDC: | 49967-371 |
| Proprietary Name: | LOreal Paris Sublime Sun |
| Non Proprietary Name: | Avobenzone Homosalate Octisalate Octocrylene Oxybenzone |
| Active Ingredient(s): | 1.5; 7.5; 2.5; 2.5; 3 mL/50mL; mL/50mL; mL/50mL; mL/50mL; mL/50mL & nbsp; Avobenzone Homosalate Octisalate Octocrylene Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LOreal Paris Sublime Sun
| Product NDC: | 49967-371 |
| Labeler Name: | L'Oreal USA Products Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111001 |
Package Information of LOreal Paris Sublime Sun
| Package NDC: | 49967-371-01 |
| Package Description: | 50 mL in 1 TUBE (49967-371-01) |
NDC Information of LOreal Paris Sublime Sun
| NDC Code | 49967-371-01 |
| Proprietary Name | LOreal Paris Sublime Sun |
| Package Description | 50 mL in 1 TUBE (49967-371-01) |
| Product NDC | 49967-371 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone Homosalate Octisalate Octocrylene Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20111001 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | L'Oreal USA Products Inc |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 1.5; 7.5; 2.5; 2.5; 3 |
| Strength Unit | mL/50mL; mL/50mL; mL/50mL; mL/50mL; mL/50mL |
| Pharmaceutical Classes |
