| Product NDC: | 53208-515 |
| Proprietary Name: | OHUI THE FIRST CELL REVOLUTION AGE CONTROL SUN BLOCK |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, ENSULIZOLE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE |
| Active Ingredient(s): | .5; 3.9; .5; 7; 4.8; 6 g/100g; g/100g; g/100g; g/100g; g/100g; g/100g & nbsp; OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, ENSULIZOLE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 53208-515 |
| Labeler Name: | LG Household and Healthcare, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110406 |
| Package NDC: | 53208-515-02 |
| Package Description: | 1 CONTAINER in 1 BOX (53208-515-02) > 40 g in 1 CONTAINER (53208-515-01) |
| NDC Code | 53208-515-02 |
| Proprietary Name | OHUI THE FIRST CELL REVOLUTION AGE CONTROL SUN BLOCK |
| Package Description | 1 CONTAINER in 1 BOX (53208-515-02) > 40 g in 1 CONTAINER (53208-515-01) |
| Product NDC | 53208-515 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, ENSULIZOLE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110406 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | LG Household and Healthcare, Inc. |
| Substance Name | DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE; ENSULIZOLE; HYDROXYPROLINE; OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE |
| Strength Number | .5; 3.9; .5; 7; 4.8; 6 |
| Strength Unit | g/100g; g/100g; g/100g; g/100g; g/100g; g/100g |
| Pharmaceutical Classes |