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Kiehls Since 1851 CrossTerrain UV Skin Protector
Kiehls Since 1851 CrossTerrain UV Skin Protector - 49967-382-01 - (Avobenzone Homosalate Octisalate Octocrylene Oxybenzone)
Drug Information of Kiehls Since 1851 CrossTerrain UV Skin Protector
| Product NDC: | 49967-382 |
| Proprietary Name: | Kiehls Since 1851 CrossTerrain UV Skin Protector |
| Non Proprietary Name: | Avobenzone Homosalate Octisalate Octocrylene Oxybenzone |
| Active Ingredient(s): | 1.2; 4; 2; 3; 2 g/40g; g/40g; g/40g; g/40g; g/40g & nbsp; Avobenzone Homosalate Octisalate Octocrylene Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Kiehls Since 1851 CrossTerrain UV Skin Protector
| Product NDC: | 49967-382 |
| 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: | 20100601 |
Package Information of Kiehls Since 1851 CrossTerrain UV Skin Protector
| Package NDC: | 49967-382-01 |
| Package Description: | 40 g in 1 JAR (49967-382-01) |
NDC Information of Kiehls Since 1851 CrossTerrain UV Skin Protector
| NDC Code | 49967-382-01 |
| Proprietary Name | Kiehls Since 1851 CrossTerrain UV Skin Protector |
| Package Description | 40 g in 1 JAR (49967-382-01) |
| Product NDC | 49967-382 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone Homosalate Octisalate Octocrylene Oxybenzone |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20100601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | L'Oreal USA Products Inc |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 1.2; 4; 2; 3; 2 |
| Strength Unit | g/40g; g/40g; g/40g; g/40g; g/40g |
| Pharmaceutical Classes |
