Product NDC: | 52000-004 |
Proprietary Name: | Allure Ice Cold Analgesic |
Non Proprietary Name: | Menthol and Camphor |
Active Ingredient(s): | .5; 1 g/100g; g/100g & nbsp; Menthol and Camphor |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52000-004 |
Labeler Name: | Universal Distribution Center LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120630 |
Package NDC: | 52000-004-18 |
Package Description: | 170 g in 1 TUBE (52000-004-18) |
NDC Code | 52000-004-18 |
Proprietary Name | Allure Ice Cold Analgesic |
Package Description | 170 g in 1 TUBE (52000-004-18) |
Product NDC | 52000-004 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Menthol and Camphor |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20120630 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Universal Distribution Center LLC |
Substance Name | CAMPHOR (SYNTHETIC); MENTHOL |
Strength Number | .5; 1 |
Strength Unit | g/100g; g/100g |
Pharmaceutical Classes |