Product NDC: | 75974-100 |
Proprietary Name: | ANC Neverpain External Analgesic |
Non Proprietary Name: | MENTHOL |
Active Ingredient(s): | 5 mL/100mL & nbsp; MENTHOL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 75974-100 |
Labeler Name: | ANC Amazon Natural Corp. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110324 |
Package NDC: | 75974-100-02 |
Package Description: | 59 mL in 1 BOTTLE, SPRAY (75974-100-02) |
NDC Code | 75974-100-02 |
Proprietary Name | ANC Neverpain External Analgesic |
Package Description | 59 mL in 1 BOTTLE, SPRAY (75974-100-02) |
Product NDC | 75974-100 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | MENTHOL |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20110324 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | ANC Amazon Natural Corp. |
Substance Name | MENTHOL |
Strength Number | 5 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |