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MOISTURIZING SUNSCREEN SPF15
MOISTURIZING SUNSCREEN SPF15 - 59663-001-01 - (OXYBENZONE)
Drug Information of MOISTURIZING SUNSCREEN SPF15
| Product NDC: | 59663-001 |
| Proprietary Name: | MOISTURIZING SUNSCREEN SPF15 |
| Non Proprietary Name: | OXYBENZONE |
| Active Ingredient(s): | 1; 1 mL/200mL; mL/100mL & nbsp; OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MOISTURIZING SUNSCREEN SPF15
| Product NDC: | 59663-001 |
| Labeler Name: | Shine & Pretty (USA), Corp. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19960202 |
Package Information of MOISTURIZING SUNSCREEN SPF15
| Package NDC: | 59663-001-01 |
| Package Description: | 100 mL in 1 BOTTLE (59663-001-01) |
NDC Information of MOISTURIZING SUNSCREEN SPF15
| NDC Code | 59663-001-01 |
| Proprietary Name | MOISTURIZING SUNSCREEN SPF15 |
| Package Description | 100 mL in 1 BOTTLE (59663-001-01) |
| Product NDC | 59663-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OXYBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19960202 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Shine & Pretty (USA), Corp. |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | 1; 1 |
| Strength Unit | mL/200mL; mL/100mL |
| Pharmaceutical Classes |
