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Derma Blemish Stick SPF50
Derma Blemish Stick SPF50 - 76344-5001-2 - (TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE)
Drug Information of Derma Blemish Stick SPF50
| Product NDC: | 76344-5001 |
| Proprietary Name: | Derma Blemish Stick SPF50 |
| Non Proprietary Name: | TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE |
| Active Ingredient(s): | 7; 18.9; 4.8 g/100g; g/100g; g/100g & nbsp; TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Derma Blemish Stick SPF50
| Product NDC: | 76344-5001 |
| Labeler Name: | Humex,Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130515 |
Package Information of Derma Blemish Stick SPF50
| Package NDC: | 76344-5001-2 |
| Package Description: | 1 CYLINDER in 1 BOX (76344-5001-2) > 9.5 g in 1 CYLINDER (76344-5001-1) |
NDC Information of Derma Blemish Stick SPF50
| NDC Code | 76344-5001-2 |
| Proprietary Name | Derma Blemish Stick SPF50 |
| Package Description | 1 CYLINDER in 1 BOX (76344-5001-2) > 9.5 g in 1 CYLINDER (76344-5001-1) |
| Product NDC | 76344-5001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20130515 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Humex,Inc. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 7; 18.9; 4.8 |
| Strength Unit | g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
