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QUINCE WHITENING SUN
QUINCE WHITENING SUN - 76214-031-01 - (OCTINOXATE)
Drug Information of QUINCE WHITENING SUN
| Product NDC: | 76214-031 |
| Proprietary Name: | QUINCE WHITENING SUN |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | 4.9; 3.5; .65 mL/70mL; mL/70mL; mL/70mL & nbsp; OCTINOXATE |
| Administration Route(s): | CUTANEOUS |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of QUINCE WHITENING SUN
| Product NDC: | 76214-031 |
| 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 QUINCE WHITENING SUN
| Package NDC: | 76214-031-01 |
| Package Description: | 70 mL in 1 BOTTLE (76214-031-01) |
NDC Information of QUINCE WHITENING SUN
| NDC Code | 76214-031-01 |
| Proprietary Name | QUINCE WHITENING SUN |
| Package Description | 70 mL in 1 BOTTLE (76214-031-01) |
| Product NDC | 76214-031 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | LOTION |
| Route Name | CUTANEOUS |
| Start Marketing Date | 20110301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | SKINFOOD CO., LTD. |
| Substance Name | OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE |
| Strength Number | 4.9; 3.5; .65 |
| Strength Unit | mL/70mL; mL/70mL; mL/70mL |
| Pharmaceutical Classes |
