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Analgesic
Analgesic - 76417-8200-1 - (menthol)
Drug Information of Analgesic
| Product NDC: | 76417-8200 |
| Proprietary Name: | Analgesic |
| Non Proprietary Name: | menthol |
| Active Ingredient(s): | 700 mL/L & nbsp; menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Analgesic
| Product NDC: | 76417-8200 |
| Labeler Name: | Ouwee Jones, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111026 |
Package Information of Analgesic
| Package NDC: | 76417-8200-1 |
| Package Description: | .118 L in 1 BOTTLE, SPRAY (76417-8200-1) |
NDC Information of Analgesic
| NDC Code | 76417-8200-1 |
| Proprietary Name | Analgesic |
| Package Description | .118 L in 1 BOTTLE, SPRAY (76417-8200-1) |
| Product NDC | 76417-8200 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | menthol |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20111026 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ouwee Jones, LLC |
| Substance Name | MENTHOL |
| Strength Number | 700 |
| Strength Unit | mL/L |
| Pharmaceutical Classes |
