Product NDC: | 22431-359 |
Proprietary Name: | Relief MD |
Non Proprietary Name: | Colloidal Oatmeal |
Active Ingredient(s): | 1 g/g & nbsp; Colloidal Oatmeal |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GRANULE, EFFERVESCENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 22431-359 |
Labeler Name: | Blue Cross Laboratories, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100917 |
Package NDC: | 22431-359-02 |
Package Description: | 6 PACKET in 1 BOX (22431-359-02) > 42.5 g in 1 PACKET (22431-359-01) |
NDC Code | 22431-359-02 |
Proprietary Name | Relief MD |
Package Description | 6 PACKET in 1 BOX (22431-359-02) > 42.5 g in 1 PACKET (22431-359-01) |
Product NDC | 22431-359 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Colloidal Oatmeal |
Dosage Form Name | GRANULE, EFFERVESCENT |
Route Name | TOPICAL |
Start Marketing Date | 20100917 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Blue Cross Laboratories, Inc. |
Substance Name | OATMEAL |
Strength Number | 1 |
Strength Unit | g/g |
Pharmaceutical Classes |