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Pain Relief
Pain Relief - 76029-001-02 - (Ruta Graveolens)
Drug Information of Pain Relief
| Product NDC: | 76029-001 |
| Proprietary Name: | Pain Relief |
| Non Proprietary Name: | Ruta Graveolens |
| Active Ingredient(s): | 3 [hp_X]/50g & nbsp; Ruta Graveolens |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pain Relief
| Product NDC: | 76029-001 |
| Labeler Name: | Active Release Techniques LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20110401 |
Package Information of Pain Relief
| Package NDC: | 76029-001-02 |
| Package Description: | 50 g in 1 CONTAINER (76029-001-02) |
NDC Information of Pain Relief
| NDC Code | 76029-001-02 |
| Proprietary Name | Pain Relief |
| Package Description | 50 g in 1 CONTAINER (76029-001-02) |
| Product NDC | 76029-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ruta Graveolens |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110401 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Active Release Techniques LLC |
| Substance Name | RUTA GRAVEOLENS FLOWERING TOP |
| Strength Number | 3 |
| Strength Unit | [hp_X]/50g |
| Pharmaceutical Classes |
