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NDC 17312-0171-14 Fibromyalgia Relief 6; 6; 6; 6; 6; 6 [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1 Details
Fibromyalgia Relief 6; 6; 6; 6; 6; 6 [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1
Fibromyalgia Relief is a ORAL TABLET, ORALLY DISINTEGRATING in the HUMAN OTC DRUG category. It is labeled and distributed by TRP Company. The primary component is BRYONIA ALBA ROOT; CAUSTICUM; LOESELIA MEXICANA WHOLE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PULSATILLA VULGARIS; TOXICODENDRON PUBESCENS LEAF.
Product Information
| NDC | 17312-0171 |
|---|---|
| Product ID | 17312-171_f1ed7811-cdca-23f4-e053-2a95a90af36b |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Fibromyalgia Relief |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | BRYONIA ALBA ROOT - CAUSTICUM - LOESELIA MEXICANA WHOLE - MAGNESIUM PHOSPHATE - PULSATILLA VULGARIS - TOXICODENDRON PUBESCENS LEAF - VALERIAN |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, ORALLY DISINTEGRATING |
| Route | ORAL |
| Active Ingredient Strength | 6; 6; 6; 6; 6; 6 |
| Active Ingredient Units | [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1 |
| Substance Name | BRYONIA ALBA ROOT; CAUSTICUM; LOESELIA MEXICANA WHOLE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PULSATILLA VULGARIS; TOXICODENDRON PUBESCENS LEAF |
| Labeler Name | TRP Company |
| Pharmaceutical Class | Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED HOMEOPATHIC |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 17312-0171-14 (17312017114)
| NDC Package Code | 17312-171-14 |
|---|---|
| Billing NDC | 17312017114 |
| Package | 1 BOTTLE in 1 PACKAGE (17312-171-14) / 70 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE |
| Marketing Start Date | 2020-05-28 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |