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EOUX
EOUX - 66854-009-01 - (ALUMINUM CHLOROHYDRATE)
Drug Information of EOUX
| Product NDC: | 66854-009 |
| Proprietary Name: | EOUX |
| Non Proprietary Name: | ALUMINUM CHLOROHYDRATE |
| Active Ingredient(s): | 280 mL/1000mL & nbsp; ALUMINUM CHLOROHYDRATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EOUX
| Product NDC: | 66854-009 |
| Labeler Name: | SPAI SONS PHARMACEUTICAL INTERNATIONAL COSMETICS |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120531 |
Package Information of EOUX
| Package NDC: | 66854-009-01 |
| Package Description: | 90 mL in 1 JAR (66854-009-01) |
NDC Information of EOUX
| NDC Code | 66854-009-01 |
| Proprietary Name | EOUX |
| Package Description | 90 mL in 1 JAR (66854-009-01) |
| Product NDC | 66854-009 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALUMINUM CHLOROHYDRATE |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120531 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | SPAI SONS PHARMACEUTICAL INTERNATIONAL COSMETICS |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | 280 |
| Strength Unit | mL/1000mL |
| Pharmaceutical Classes |
