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Cold Spot
Cold Spot - 65121-001-04 - (menthol)
Drug Information of Cold Spot
| Product NDC: | 65121-001 |
| Proprietary Name: | Cold Spot |
| Non Proprietary Name: | menthol |
| Active Ingredient(s): | .46 L/3.8L & nbsp; menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cold Spot
| Product NDC: | 65121-001 |
| Labeler Name: | Pure Source |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100824 |
Package Information of Cold Spot
| Package NDC: | 65121-001-04 |
| Package Description: | 120 mL in 1 TUBE (65121-001-04) |
NDC Information of Cold Spot
| NDC Code | 65121-001-04 |
| Proprietary Name | Cold Spot |
| Package Description | 120 mL in 1 TUBE (65121-001-04) |
| Product NDC | 65121-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | menthol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100824 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pure Source |
| Substance Name | MENTHOL |
| Strength Number | .46 |
| Strength Unit | L/3.8L |
| Pharmaceutical Classes |
