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PHYLLIS GOLDEN
PHYLLIS GOLDEN - 52841-020-01 - (OATMEAL)
Drug Information of PHYLLIS GOLDEN
| Product NDC: | 52841-020 |
| Proprietary Name: | PHYLLIS GOLDEN |
| Non Proprietary Name: | OATMEAL |
| Active Ingredient(s): | .0008 mL/80mL & nbsp; OATMEAL |
| Administration Route(s): | CUTANEOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PHYLLIS GOLDEN
| Product NDC: | 52841-020 |
| Labeler Name: | UNOCOS CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100401 |
Package Information of PHYLLIS GOLDEN
| Package NDC: | 52841-020-01 |
| Package Description: | 80 mL in 1 CARTON (52841-020-01) |
NDC Information of PHYLLIS GOLDEN
| NDC Code | 52841-020-01 |
| Proprietary Name | PHYLLIS GOLDEN |
| Package Description | 80 mL in 1 CARTON (52841-020-01) |
| Product NDC | 52841-020 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OATMEAL |
| Dosage Form Name | SOLUTION |
| Route Name | CUTANEOUS |
| Start Marketing Date | 20100401 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | UNOCOS CO., LTD. |
| Substance Name | OATMEAL |
| Strength Number | .0008 |
| Strength Unit | mL/80mL |
| Pharmaceutical Classes |
