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PURE SPRING
PURE SPRING - 11822-4670-9 - (ETHYL ALCOHOL)
Drug Information of PURE SPRING
| Product NDC: | 11822-4670 |
| Proprietary Name: | PURE SPRING |
| Non Proprietary Name: | ETHYL ALCOHOL |
| Active Ingredient(s): | 62 mL/100mL & nbsp; ETHYL ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PURE SPRING
| Product NDC: | 11822-4670 |
| Labeler Name: | RITE AID CORPORATION |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120319 |
Package Information of PURE SPRING
| Package NDC: | 11822-4670-9 |
| Package Description: | 260 mL in 1 BOTTLE, PLASTIC (11822-4670-9) |
NDC Information of PURE SPRING
| NDC Code | 11822-4670-9 |
| Proprietary Name | PURE SPRING |
| Package Description | 260 mL in 1 BOTTLE, PLASTIC (11822-4670-9) |
| Product NDC | 11822-4670 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ETHYL ALCOHOL |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120319 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | RITE AID CORPORATION |
| Substance Name | ALCOHOL |
| Strength Number | 62 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
