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Cold Spot
Cold Spot - 51452-005-04 - (MENTHOL)
Drug Information of Cold Spot
| Product NDC: | 51452-005 |
| Proprietary Name: | Cold Spot |
| Non Proprietary Name: | MENTHOL |
| Active Ingredient(s): | 14.4; 4.8 mL/120mL; mL/120mL & nbsp; MENTHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cold Spot
| Product NDC: | 51452-005 |
| Labeler Name: | Fabrication Enterprises, inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111013 |
Package Information of Cold Spot
| Package NDC: | 51452-005-04 |
| Package Description: | 4 mL in 1 TUBE, WITH APPLICATOR (51452-005-04) |
NDC Information of Cold Spot
| NDC Code | 51452-005-04 |
| Proprietary Name | Cold Spot |
| Package Description | 4 mL in 1 TUBE, WITH APPLICATOR (51452-005-04) |
| Product NDC | 51452-005 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MENTHOL |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20111013 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Fabrication Enterprises, inc. |
| Substance Name | MENTHOL; METHYL SALICYLATE |
| Strength Number | 14.4; 4.8 |
| Strength Unit | mL/120mL; mL/120mL |
| Pharmaceutical Classes |
