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ActivOn Ultra Strength Arthritis
ActivOn Ultra Strength Arthritis - 51068-501-01 - (Menthol and Histamine Dihydrochloride)
Drug Information of ActivOn Ultra Strength Arthritis
| Product NDC: | 51068-501 |
| Proprietary Name: | ActivOn Ultra Strength Arthritis |
| Non Proprietary Name: | Menthol and Histamine Dihydrochloride |
| Active Ingredient(s): | .00028; .04574 g/g; g/g & nbsp; Menthol and Histamine Dihydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ActivOn Ultra Strength Arthritis
| Product NDC: | 51068-501 |
| Labeler Name: | Family First Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110901 |
Package Information of ActivOn Ultra Strength Arthritis
| Package NDC: | 51068-501-01 |
| Package Description: | 1 CANISTER in 1 CARTON (51068-501-01) > 57 g in 1 CANISTER |
NDC Information of ActivOn Ultra Strength Arthritis
| NDC Code | 51068-501-01 |
| Proprietary Name | ActivOn Ultra Strength Arthritis |
| Package Description | 1 CANISTER in 1 CARTON (51068-501-01) > 57 g in 1 CANISTER |
| Product NDC | 51068-501 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol and Histamine Dihydrochloride |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20110901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Family First Pharmaceuticals, Inc. |
| Substance Name | HISTAMINE DIHYDROCHLORIDE; MENTHOL |
| Strength Number | .00028; .04574 |
| Strength Unit | g/g; g/g |
| Pharmaceutical Classes |
