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Sunscreen Mango and Coconut
Sunscreen Mango and Coconut - 55118-600-11 - (Avobenzone, Octinoxate, Octisalate, Octocrylene, and Oxybenzone)
Drug Information of Sunscreen Mango and Coconut
| Product NDC: | 55118-600 |
| Proprietary Name: | Sunscreen Mango and Coconut |
| Non Proprietary Name: | Avobenzone, Octinoxate, Octisalate, Octocrylene, and Oxybenzone |
| Active Ingredient(s): | 10; 75; 50; 8; 50 mg/g; mg/g; mg/g; mg/g; mg/g & nbsp; Avobenzone, Octinoxate, Octisalate, Octocrylene, and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunscreen Mango and Coconut
| Product NDC: | 55118-600 |
| Labeler Name: | Kimberly-Clark Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100315 |
Package Information of Sunscreen Mango and Coconut
| Package NDC: | 55118-600-11 |
| Package Description: | 45 g in 1 BOTTLE, PLASTIC (55118-600-11) |
NDC Information of Sunscreen Mango and Coconut
| NDC Code | 55118-600-11 |
| Proprietary Name | Sunscreen Mango and Coconut |
| Package Description | 45 g in 1 BOTTLE, PLASTIC (55118-600-11) |
| Product NDC | 55118-600 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate, Octisalate, Octocrylene, and Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100315 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Kimberly-Clark Corporation |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 10; 75; 50; 8; 50 |
| Strength Unit | mg/g; mg/g; mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
