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Blue Ice Analgesic
Blue Ice Analgesic - 61734-021-03 - (Menthol)
Drug Information of Blue Ice Analgesic
| Product NDC: | 61734-021 |
| Proprietary Name: | Blue Ice Analgesic |
| Non Proprietary Name: | Menthol |
| Active Ingredient(s): | 2 g/100g & nbsp; Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Blue Ice Analgesic
| Product NDC: | 61734-021 |
| Labeler Name: | Delon Laboratories (1990) Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100507 |
Package Information of Blue Ice Analgesic
| Package NDC: | 61734-021-03 |
| Package Description: | 227 g in 1 CONTAINER (61734-021-03) |
NDC Information of Blue Ice Analgesic
| NDC Code | 61734-021-03 |
| Proprietary Name | Blue Ice Analgesic |
| Package Description | 227 g in 1 CONTAINER (61734-021-03) |
| Product NDC | 61734-021 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100507 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Delon Laboratories (1990) Ltd |
| Substance Name | MENTHOL |
| Strength Number | 2 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
