| Product NDC: | 43419-354 |
| Proprietary Name: | IOPE S.S. CONDITIONING COLOR BASE No.40 |
| Non Proprietary Name: | Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE |
| Active Ingredient(s): | .05; .0439; .0098 mL/mL; mL/mL; mL/mL & nbsp; Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 43419-354 |
| Labeler Name: | AMOREPACIFIC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20101101 |
| Package NDC: | 43419-354-01 |
| Package Description: | 35 mL in 1 BOTTLE (43419-354-01) |
| NDC Code | 43419-354-01 |
| Proprietary Name | IOPE S.S. CONDITIONING COLOR BASE No.40 |
| Package Description | 35 mL in 1 BOTTLE (43419-354-01) |
| Product NDC | 43419-354 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20101101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | AMOREPACIFIC |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | .05; .0439; .0098 |
| Strength Unit | mL/mL; mL/mL; mL/mL |
| Pharmaceutical Classes |