Product NDC: | 65121-496 |
Proprietary Name: | Frankie Avalons ZERO PAIN Original Formula Roll-On Maximum Strength PAIN RELIEVER |
Non Proprietary Name: | CAPSAICIN |
Active Ingredient(s): | .25 mg/mL & nbsp; CAPSAICIN |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65121-496 |
Labeler Name: | Pure Source Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130710 |
Package NDC: | 65121-496-04 |
Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 BOX (65121-496-04) > 90 mL in 1 BOTTLE, WITH APPLICATOR |
NDC Code | 65121-496-04 |
Proprietary Name | Frankie Avalons ZERO PAIN Original Formula Roll-On Maximum Strength PAIN RELIEVER |
Package Description | 1 BOTTLE, WITH APPLICATOR in 1 BOX (65121-496-04) > 90 mL in 1 BOTTLE, WITH APPLICATOR |
Product NDC | 65121-496 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | CAPSAICIN |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20130710 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Pure Source Inc. |
Substance Name | CAPSAICIN |
Strength Number | .25 |
Strength Unit | mg/mL |
Pharmaceutical Classes |