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MediSpa Sunspray (sunblock)
MediSpa Sunspray (sunblock) - 76344-2001-2 - (OCTINOXATE, AMILOXATE, BEMOTRIZINOL, TITANIUM DIOXIDE)
Drug Information of MediSpa Sunspray (sunblock)
| Product NDC: | 76344-2001 |
| Proprietary Name: | MediSpa Sunspray (sunblock) |
| Non Proprietary Name: | OCTINOXATE, AMILOXATE, BEMOTRIZINOL, TITANIUM DIOXIDE |
| Active Ingredient(s): | 2; 2; 7.5; 1.4 g/100mL; g/100mL; g/100mL; g/100mL & nbsp; OCTINOXATE, AMILOXATE, BEMOTRIZINOL, TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MediSpa Sunspray (sunblock)
| Product NDC: | 76344-2001 |
| Labeler Name: | Humex,Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130329 |
Package Information of MediSpa Sunspray (sunblock)
| Package NDC: | 76344-2001-2 |
| Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 BOX (76344-2001-2) > 55 mL in 1 BOTTLE, WITH APPLICATOR (76344-2001-1) |
NDC Information of MediSpa Sunspray (sunblock)
| NDC Code | 76344-2001-2 |
| Proprietary Name | MediSpa Sunspray (sunblock) |
| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 BOX (76344-2001-2) > 55 mL in 1 BOTTLE, WITH APPLICATOR (76344-2001-1) |
| Product NDC | 76344-2001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, AMILOXATE, BEMOTRIZINOL, TITANIUM DIOXIDE |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20130329 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Humex,Inc. |
| Substance Name | AMILOXATE; BEMOTRIZINOL; OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 2; 2; 7.5; 1.4 |
| Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |
