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PAIN RELIEVER
PAIN RELIEVER - 35192-002-02 - (MENTHOL)
Drug Information of PAIN RELIEVER
| Product NDC: | 35192-002 |
| Proprietary Name: | PAIN RELIEVER |
| Non Proprietary Name: | MENTHOL |
| Active Ingredient(s): | 2.4 g/120g & nbsp; MENTHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PAIN RELIEVER
| Product NDC: | 35192-002 |
| Labeler Name: | CA-BOTANA INTERNATIONAL |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110824 |
Package Information of PAIN RELIEVER
| Package NDC: | 35192-002-02 |
| Package Description: | 120 g in 1 TUBE (35192-002-02) |
NDC Information of PAIN RELIEVER
| NDC Code | 35192-002-02 |
| Proprietary Name | PAIN RELIEVER |
| Package Description | 120 g in 1 TUBE (35192-002-02) |
| Product NDC | 35192-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MENTHOL |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20110824 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CA-BOTANA INTERNATIONAL |
| Substance Name | MENTHOL |
| Strength Number | 2.4 |
| Strength Unit | g/120g |
| Pharmaceutical Classes |
