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DERMAPROT
DERMAPROT - 66854-026-03 - (OCTINOXATE,TITANIUM DIOXIDE,OXYBENZONE,AVOBENZONE)
Drug Information of DERMAPROT
| Product NDC: | 66854-026 |
| Proprietary Name: | DERMAPROT |
| Non Proprietary Name: | OCTINOXATE,TITANIUM DIOXIDE,OXYBENZONE,AVOBENZONE |
| Active Ingredient(s): | 2.5; 7.5; 1.5; 3 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE,TITANIUM DIOXIDE,OXYBENZONE,AVOBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DERMAPROT
| Product NDC: | 66854-026 |
| Labeler Name: | SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120630 |
Package Information of DERMAPROT
| Package NDC: | 66854-026-03 |
| Package Description: | 70 mL in 1 BOTTLE (66854-026-03) |
NDC Information of DERMAPROT
| NDC Code | 66854-026-03 |
| Proprietary Name | DERMAPROT |
| Package Description | 70 mL in 1 BOTTLE (66854-026-03) |
| Product NDC | 66854-026 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE,TITANIUM DIOXIDE,OXYBENZONE,AVOBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120630 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS |
| Substance Name | AVOBENZONE; OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE |
| Strength Number | 2.5; 7.5; 1.5; 3 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
