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Wild Country
Wild Country - 10096-9298-1 - (ALUMINUM CHLOROHYDRATE)
Drug Information of Wild Country
| Product NDC: | 10096-9298 |
| Proprietary Name: | Wild Country |
| Non Proprietary Name: | ALUMINUM CHLOROHYDRATE |
| Active Ingredient(s): | 145 mg/mL & nbsp; ALUMINUM CHLOROHYDRATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Wild Country
| Product NDC: | 10096-9298 |
| Labeler Name: | Avon Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121114 |
Package Information of Wild Country
| Package NDC: | 10096-9298-1 |
| Package Description: | 50 mL in 1 BOTTLE, DISPENSING (10096-9298-1) |
NDC Information of Wild Country
| NDC Code | 10096-9298-1 |
| Proprietary Name | Wild Country |
| Package Description | 50 mL in 1 BOTTLE, DISPENSING (10096-9298-1) |
| Product NDC | 10096-9298 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALUMINUM CHLOROHYDRATE |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20121114 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Avon Products, Inc. |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | 145 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
