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Flexall Pain Relieving
Flexall Pain Relieving - 21695-642-03 - (Menthol)
Drug Information of Flexall Pain Relieving
| Product NDC: | 21695-642 |
| Proprietary Name: | Flexall Pain Relieving |
| Non Proprietary Name: | Menthol |
| Active Ingredient(s): | .16 g/g & nbsp; Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Flexall Pain Relieving
| Product NDC: | 21695-642 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19970101 |
Package Information of Flexall Pain Relieving
| Package NDC: | 21695-642-03 |
| Package Description: | 1 TUBE in 1 CARTON (21695-642-03) > 85 g in 1 TUBE |
NDC Information of Flexall Pain Relieving
| NDC Code | 21695-642-03 |
| Proprietary Name | Flexall Pain Relieving |
| Package Description | 1 TUBE in 1 CARTON (21695-642-03) > 85 g in 1 TUBE |
| Product NDC | 21695-642 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 19970101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | MENTHOL |
| Strength Number | .16 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
