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UV LOCK ULTRA PACT SUN
UV LOCK ULTRA PACT SUN - 51346-041-01 - (TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE)
Drug Information of UV LOCK ULTRA PACT SUN
| Product NDC: | 51346-041 |
| Proprietary Name: | UV LOCK ULTRA PACT SUN |
| Non Proprietary Name: | TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE |
| Active Ingredient(s): | .24; .62; .23 g/8g; g/8g; g/8g & nbsp; TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of UV LOCK ULTRA PACT SUN
| Product NDC: | 51346-041 |
| Labeler Name: | NATURE REPUBLIC CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120102 |
Package Information of UV LOCK ULTRA PACT SUN
| Package NDC: | 51346-041-01 |
| Package Description: | 8 g in 1 CARTON (51346-041-01) |
NDC Information of UV LOCK ULTRA PACT SUN
| NDC Code | 51346-041-01 |
| Proprietary Name | UV LOCK ULTRA PACT SUN |
| Package Description | 8 g in 1 CARTON (51346-041-01) |
| Product NDC | 51346-041 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20120102 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | NATURE REPUBLIC CO., LTD. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | .24; .62; .23 |
| Strength Unit | g/8g; g/8g; g/8g |
| Pharmaceutical Classes |
