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Phoenix Balm
Phoenix Balm - 24438-001-02 - (Pain Relief Rub)
Drug Information of Phoenix Balm
| Product NDC: | 24438-001 |
| Proprietary Name: | Phoenix Balm |
| Non Proprietary Name: | Pain Relief Rub |
| Active Ingredient(s): | 50; 50; 50 mg/g; mg/g; mg/g & nbsp; Pain Relief Rub |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phoenix Balm
| Product NDC: | 24438-001 |
| Labeler Name: | Amazonian Naturals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111201 |
Package Information of Phoenix Balm
| Package NDC: | 24438-001-02 |
| Package Description: | 1 CONTAINER in 1 BOX (24438-001-02) > 19 g in 1 CONTAINER (24438-001-01) |
NDC Information of Phoenix Balm
| NDC Code | 24438-001-02 |
| Proprietary Name | Phoenix Balm |
| Package Description | 1 CONTAINER in 1 BOX (24438-001-02) > 19 g in 1 CONTAINER (24438-001-01) |
| Product NDC | 24438-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pain Relief Rub |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20111201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Amazonian Naturals, Inc. |
| Substance Name | CAMPHOR (NATURAL); MENTHOL; METHYL SALICYLATE |
| Strength Number | 50; 50; 50 |
| Strength Unit | mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
