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DOCTOR HOYS NATURAL PAIN RELIEF
DOCTOR HOYS NATURAL PAIN RELIEF - 10842-212-01 - (CAMPHOR MENTHOL)
Drug Information of DOCTOR HOYS NATURAL PAIN RELIEF
| Product NDC: | 10842-212 |
| Proprietary Name: | DOCTOR HOYS NATURAL PAIN RELIEF |
| Non Proprietary Name: | CAMPHOR MENTHOL |
| Active Ingredient(s): | 5; 5 g/100mL; g/100mL & nbsp; CAMPHOR MENTHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DOCTOR HOYS NATURAL PAIN RELIEF
| Product NDC: | 10842-212 |
| Labeler Name: | DOCTOR HOY'S, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120701 |
Package Information of DOCTOR HOYS NATURAL PAIN RELIEF
| Package NDC: | 10842-212-01 |
| Package Description: | 119 mL in 1 TUBE (10842-212-01) |
NDC Information of DOCTOR HOYS NATURAL PAIN RELIEF
| NDC Code | 10842-212-01 |
| Proprietary Name | DOCTOR HOYS NATURAL PAIN RELIEF |
| Package Description | 119 mL in 1 TUBE (10842-212-01) |
| Product NDC | 10842-212 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CAMPHOR MENTHOL |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20120701 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | DOCTOR HOY'S, LLC |
| Substance Name | CAMPHOR (NATURAL); MENTHOL |
| Strength Number | 5; 5 |
| Strength Unit | g/100mL; g/100mL |
| Pharmaceutical Classes |
