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BIOWHITE BRIGHTENING
BIOWHITE BRIGHTENING - 44781-160-01 - (DIMETHICONE)
Drug Information of BIOWHITE BRIGHTENING
| Product NDC: | 44781-160 |
| Proprietary Name: | BIOWHITE BRIGHTENING |
| Non Proprietary Name: | DIMETHICONE |
| Active Ingredient(s): | .5 mL/50mL & nbsp; DIMETHICONE |
| Administration Route(s): | CUTANEOUS |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BIOWHITE BRIGHTENING
| Product NDC: | 44781-160 |
| Labeler Name: | ZION SYNTHETIC FIBER CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100401 |
Package Information of BIOWHITE BRIGHTENING
| Package NDC: | 44781-160-01 |
| Package Description: | 50 mL in 1 CARTON (44781-160-01) |
NDC Information of BIOWHITE BRIGHTENING
| NDC Code | 44781-160-01 |
| Proprietary Name | BIOWHITE BRIGHTENING |
| Package Description | 50 mL in 1 CARTON (44781-160-01) |
| Product NDC | 44781-160 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIMETHICONE |
| Dosage Form Name | CREAM |
| Route Name | CUTANEOUS |
| Start Marketing Date | 20100401 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | ZION SYNTHETIC FIBER CO., LTD. |
| Substance Name | DIMETHICONE |
| Strength Number | .5 |
| Strength Unit | mL/50mL |
| Pharmaceutical Classes |
