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Kroger Sunscreen
Kroger Sunscreen - 30142-925-56 - (OCTINOXATE OXYBENZONE)
Drug Information of Kroger Sunscreen
| Product NDC: | 30142-925 |
| Proprietary Name: | Kroger Sunscreen |
| Non Proprietary Name: | OCTINOXATE OXYBENZONE |
| Active Ingredient(s): | 7.5; 2 g/100g; g/100g & nbsp; OCTINOXATE OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Kroger Sunscreen
| Product NDC: | 30142-925 |
| Labeler Name: | THE KROGER CO |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121112 |
Package Information of Kroger Sunscreen
| Package NDC: | 30142-925-56 |
| Package Description: | 226 g in 1 BOTTLE, PLASTIC (30142-925-56) |
NDC Information of Kroger Sunscreen
| NDC Code | 30142-925-56 |
| Proprietary Name | Kroger Sunscreen |
| Package Description | 226 g in 1 BOTTLE, PLASTIC (30142-925-56) |
| Product NDC | 30142-925 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE OXYBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20121112 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | THE KROGER CO |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | 7.5; 2 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |
