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Publix Sunscreen
Publix Sunscreen - 56062-700-16 - (OCTINOXATE, OXYBENZONE)
Drug Information of Publix Sunscreen
| Product NDC: | 56062-700 |
| Proprietary Name: | Publix Sunscreen |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE |
| Active Ingredient(s): | 7.5; 4.5 g/100g; g/100g & nbsp; OCTINOXATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Publix Sunscreen
| Product NDC: | 56062-700 |
| Labeler Name: | Publix Super Markets Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121114 |
Package Information of Publix Sunscreen
| Package NDC: | 56062-700-16 |
| Package Description: | 226 g in 1 BOTTLE, PLASTIC (56062-700-16) |
NDC Information of Publix Sunscreen
| NDC Code | 56062-700-16 |
| Proprietary Name | Publix Sunscreen |
| Package Description | 226 g in 1 BOTTLE, PLASTIC (56062-700-16) |
| Product NDC | 56062-700 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20121114 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Publix Super Markets Inc |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | 7.5; 4.5 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |
