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IOPE RETIGEN SMOOTHING PACT
IOPE RETIGEN SMOOTHING PACT - 43419-315-06 - (OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE)
Drug Information of IOPE RETIGEN SMOOTHING PACT
| Product NDC: | 43419-315 |
| Proprietary Name: | IOPE RETIGEN SMOOTHING PACT |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Active Ingredient(s): | .84; .86912; .4116 g/14g; g/14g; g/14g & nbsp; OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of IOPE RETIGEN SMOOTHING PACT
| Product NDC: | 43419-315 |
| Labeler Name: | AMOREPACIFIC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110801 |
Package Information of IOPE RETIGEN SMOOTHING PACT
| Package NDC: | 43419-315-06 |
| Package Description: | 14 g in 1 CONTAINER (43419-315-06) |
NDC Information of IOPE RETIGEN SMOOTHING PACT
| NDC Code | 43419-315-06 |
| Proprietary Name | IOPE RETIGEN SMOOTHING PACT |
| Package Description | 14 g in 1 CONTAINER (43419-315-06) |
| Product NDC | 43419-315 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20110801 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | AMOREPACIFIC |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | .84; .86912; .4116 |
| Strength Unit | g/14g; g/14g; g/14g |
| Pharmaceutical Classes |
