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BioRelief Ice Pain Relieving
BioRelief Ice Pain Relieving - 76019-100-02 - (MENTHOL)
Drug Information of BioRelief Ice Pain Relieving
| Product NDC: | 76019-100 |
| Proprietary Name: | BioRelief Ice Pain Relieving |
| Non Proprietary Name: | MENTHOL |
| Active Ingredient(s): | 59 mL/100mL & nbsp; MENTHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BioRelief Ice Pain Relieving
| Product NDC: | 76019-100 |
| Labeler Name: | Mekt, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110214 |
Package Information of BioRelief Ice Pain Relieving
| Package NDC: | 76019-100-02 |
| Package Description: | 1 BOTTLE in 1 CARTON (76019-100-02) > 59 mL in 1 BOTTLE |
NDC Information of BioRelief Ice Pain Relieving
| NDC Code | 76019-100-02 |
| Proprietary Name | BioRelief Ice Pain Relieving |
| Package Description | 1 BOTTLE in 1 CARTON (76019-100-02) > 59 mL in 1 BOTTLE |
| Product NDC | 76019-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MENTHOL |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20110214 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Mekt, LLC |
| Substance Name | MENTHOL |
| Strength Number | 59 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
