| 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 |