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Purell Alcohol Formulation
Purell Alcohol Formulation - 21749-367-68 - (alcohol)
Drug Information of Purell Alcohol Formulation
| Product NDC: | 21749-367 |
| Proprietary Name: | Purell Alcohol Formulation |
| Non Proprietary Name: | alcohol |
| Active Ingredient(s): | .62 mL/mL & nbsp; alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SWAB |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Purell Alcohol Formulation
| Product NDC: | 21749-367 |
| Labeler Name: | GOJO Industries, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120224 |
Package Information of Purell Alcohol Formulation
| Package NDC: | 21749-367-68 |
| Package Description: | 700 mL in 1 CANISTER (21749-367-68) |
NDC Information of Purell Alcohol Formulation
| NDC Code | 21749-367-68 |
| Proprietary Name | Purell Alcohol Formulation |
| Package Description | 700 mL in 1 CANISTER (21749-367-68) |
| Product NDC | 21749-367 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | alcohol |
| Dosage Form Name | SWAB |
| Route Name | TOPICAL |
| Start Marketing Date | 20120224 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | GOJO Industries, Inc. |
| Substance Name | ALCOHOL |
| Strength Number | .62 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
