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Sunscreen
Sunscreen - 75887-003-04 - (OCTINOXATE, OXYBENZONE)
Drug Information of Sunscreen
| Product NDC: | 75887-003 |
| Proprietary Name: | Sunscreen |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE |
| Active Ingredient(s): | 22; 16 mL/30mL; mL/30mL & nbsp; OCTINOXATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunscreen
| Product NDC: | 75887-003 |
| Labeler Name: | Aztex Enterprises |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110118 |
Package Information of Sunscreen
| Package NDC: | 75887-003-04 |
| Package Description: | 236 mL in 1 BOTTLE (75887-003-04) |
NDC Information of Sunscreen
| NDC Code | 75887-003-04 |
| Proprietary Name | Sunscreen |
| Package Description | 236 mL in 1 BOTTLE (75887-003-04) |
| Product NDC | 75887-003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110118 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Aztex Enterprises |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | 22; 16 |
| Strength Unit | mL/30mL; mL/30mL |
| Pharmaceutical Classes |
