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High Protection Sun Air Spray SPF50 PA
High Protection Sun Air Spray SPF50 PA - 43948-6001-1 - (OCTINOXATE OCTISALATE ALUMINUM HYDROXIDE)
Drug Information of High Protection Sun Air Spray SPF50 PA
| Product NDC: | 43948-6001 |
| Proprietary Name: | High Protection Sun Air Spray SPF50 PA |
| Non Proprietary Name: | OCTINOXATE OCTISALATE ALUMINUM HYDROXIDE |
| Active Ingredient(s): | 9.75 mL/130mL & nbsp; OCTINOXATE OCTISALATE ALUMINUM HYDROXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of High Protection Sun Air Spray SPF50 PA
| Product NDC: | 43948-6001 |
| Labeler Name: | The Doctor's Cosmetic Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091101 |
Package Information of High Protection Sun Air Spray SPF50 PA
| Package NDC: | 43948-6001-1 |
| Package Description: | 130 mL in 1 BOTTLE, SPRAY (43948-6001-1) |
NDC Information of High Protection Sun Air Spray SPF50 PA
| NDC Code | 43948-6001-1 |
| Proprietary Name | High Protection Sun Air Spray SPF50 PA |
| Package Description | 130 mL in 1 BOTTLE, SPRAY (43948-6001-1) |
| Product NDC | 43948-6001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE OCTISALATE ALUMINUM HYDROXIDE |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20091101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Doctor's Cosmetic Inc |
| Substance Name | OCTINOXATE |
| Strength Number | 9.75 |
| Strength Unit | mL/130mL |
| Pharmaceutical Classes |
