Product NDC: | 57367-007 |
Proprietary Name: | NICK RELIEF |
Non Proprietary Name: | ALUMINUM SULFATE |
Active Ingredient(s): | 46 mg/mL & nbsp; ALUMINUM SULFATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | STICK |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57367-007 |
Labeler Name: | 220 LABORATORIES INC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19971127 |
Package NDC: | 57367-007-20 |
Package Description: | 1 APPLICATOR in 1 BLISTER PACK (57367-007-20) > 7 mL in 1 APPLICATOR (57367-007-07) |
NDC Code | 57367-007-20 |
Proprietary Name | NICK RELIEF |
Package Description | 1 APPLICATOR in 1 BLISTER PACK (57367-007-20) > 7 mL in 1 APPLICATOR (57367-007-07) |
Product NDC | 57367-007 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALUMINUM SULFATE |
Dosage Form Name | STICK |
Route Name | TOPICAL |
Start Marketing Date | 19971127 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | 220 LABORATORIES INC |
Substance Name | ALUMINUM SULFATE |
Strength Number | 46 |
Strength Unit | mg/mL |
Pharmaceutical Classes |