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MediSpa SunSpray
MediSpa SunSpray - 52554-2001-1 - (OCTINOXATE)
Drug Information of MediSpa SunSpray
| Product NDC: | 52554-2001 |
| Proprietary Name: | MediSpa SunSpray |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | .05; .075; .01 mL/mL; mL/mL; mL/mL & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MediSpa SunSpray
| Product NDC: | 52554-2001 |
| Labeler Name: | Universal Cosmetic Co., Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100806 |
Package Information of MediSpa SunSpray
| Package NDC: | 52554-2001-1 |
| Package Description: | 55 mL in 1 BOTTLE, WITH APPLICATOR (52554-2001-1) |
NDC Information of MediSpa SunSpray
| NDC Code | 52554-2001-1 |
| Proprietary Name | MediSpa SunSpray |
| Package Description | 55 mL in 1 BOTTLE, WITH APPLICATOR (52554-2001-1) |
| Product NDC | 52554-2001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20100806 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Universal Cosmetic Co., Ltd |
| Substance Name | ENZACAMENE; OCTINOXATE; OCTOCRYLENE |
| Strength Number | .05; .075; .01 |
| Strength Unit | mL/mL; mL/mL; mL/mL |
| Pharmaceutical Classes |
