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MediSpa Sunblock
MediSpa Sunblock - 52554-1001-1 - (zinc oxide)
Drug Information of MediSpa Sunblock
| Product NDC: | 52554-1001 |
| Proprietary Name: | MediSpa Sunblock |
| Non Proprietary Name: | zinc oxide |
| Active Ingredient(s): | .005; .03; .07; .05 mL/mL; mL/mL; mL/mL; mL/mL & nbsp; zinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MediSpa Sunblock
| Product NDC: | 52554-1001 |
| Labeler Name: | Universal Cosmetic Co., Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100804 |
Package Information of MediSpa Sunblock
| Package NDC: | 52554-1001-1 |
| Package Description: | 70 mL in 1 BOTTLE, WITH APPLICATOR (52554-1001-1) |
NDC Information of MediSpa Sunblock
| NDC Code | 52554-1001-1 |
| Proprietary Name | MediSpa Sunblock |
| Package Description | 70 mL in 1 BOTTLE, WITH APPLICATOR (52554-1001-1) |
| Product NDC | 52554-1001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | zinc oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100804 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Universal Cosmetic Co., Ltd |
| Substance Name | AVOBENZONE; ENZACAMENE; OCTINOXATE; ZINC OXIDE |
| Strength Number | .005; .03; .07; .05 |
| Strength Unit | mL/mL; mL/mL; mL/mL; mL/mL |
| Pharmaceutical Classes |
