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Cold Spot
Cold Spot - 65121-002-03 - (menthol)
Drug Information of Cold Spot
| Product NDC: | 65121-002 |
| Proprietary Name: | Cold Spot |
| Non Proprietary Name: | menthol |
| Active Ingredient(s): | 13 mL/90mL & nbsp; menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cold Spot
| Product NDC: | 65121-002 |
| 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: | 65121-002-03 |
| Package Description: | 90 mL in 1 BOTTLE (65121-002-03) |
NDC Information of Cold Spot
| NDC Code | 65121-002-03 |
| Proprietary Name | Cold Spot |
| Package Description | 90 mL in 1 BOTTLE (65121-002-03) |
| Product NDC | 65121-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | menthol |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20100824 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pure Source |
| Substance Name | MENTHOL |
| Strength Number | 13 |
| Strength Unit | mL/90mL |
| Pharmaceutical Classes |
