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ULTRA STRENGTH STOPAIN PAIN RELIEVING
ULTRA STRENGTH STOPAIN PAIN RELIEVING - 63936-8508-2 - (MENTHOL)
Drug Information of ULTRA STRENGTH STOPAIN PAIN RELIEVING
| Product NDC: | 63936-8508 |
| Proprietary Name: | ULTRA STRENGTH STOPAIN PAIN RELIEVING |
| Non Proprietary Name: | MENTHOL |
| Active Ingredient(s): | 8 mL/100mL & nbsp; MENTHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ULTRA STRENGTH STOPAIN PAIN RELIEVING
| Product NDC: | 63936-8508 |
| Labeler Name: | TROY MANUFACTURING |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20101129 |
Package Information of ULTRA STRENGTH STOPAIN PAIN RELIEVING
| Package NDC: | 63936-8508-2 |
| Package Description: | 240 mL in 1 BOTTLE (63936-8508-2) |
NDC Information of ULTRA STRENGTH STOPAIN PAIN RELIEVING
| NDC Code | 63936-8508-2 |
| Proprietary Name | ULTRA STRENGTH STOPAIN PAIN RELIEVING |
| Package Description | 240 mL in 1 BOTTLE (63936-8508-2) |
| Product NDC | 63936-8508 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MENTHOL |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20101129 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | TROY MANUFACTURING |
| Substance Name | MENTHOL |
| Strength Number | 8 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
