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GOLDKIWI SUN
GOLDKIWI SUN - 76214-013-01 - (OCTINOXATE)
Drug Information of GOLDKIWI SUN
| Product NDC: | 76214-013 |
| Proprietary Name: | GOLDKIWI SUN |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | 3.75; 1.45; 2.45 g/50g; g/50g; g/50g & nbsp; OCTINOXATE |
| Administration Route(s): | CUTANEOUS |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GOLDKIWI SUN
| Product NDC: | 76214-013 |
| Labeler Name: | SKINFOOD CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110301 |
Package Information of GOLDKIWI SUN
| Package NDC: | 76214-013-01 |
| Package Description: | 50 g in 1 CARTON (76214-013-01) |
NDC Information of GOLDKIWI SUN
| NDC Code | 76214-013-01 |
| Proprietary Name | GOLDKIWI SUN |
| Package Description | 50 g in 1 CARTON (76214-013-01) |
| Product NDC | 76214-013 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | CREAM |
| Route Name | CUTANEOUS |
| Start Marketing Date | 20110301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | SKINFOOD CO., LTD. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 3.75; 1.45; 2.45 |
| Strength Unit | g/50g; g/50g; g/50g |
| Pharmaceutical Classes |
