Fibromyalgia Relief
- Product NDC
- 43689-0003
- 11-digit product format
- 436890003
- Labeler code
- 43689
- Product ID
- 43689-0003_d04145da-3e9d-423c-86b3-c0c48f3e60e8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum Napellus, Arsenicum Album, Belladonna, Coniinum, Gelsemium Sempervirens, Hypericum Perforatum, Kali Bichromicum
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- The Magni Company
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-10-11
- Marketing end
- 2023-01-14
- Substance
- ACONITUM NAPELLUS; ARSENIC TRIOXIDE; ATROPA BELLADONNA; CONIINE; GELSEMIUM SEMPERVIRENS ROOT; HYPERICUM PERFORATUM; LACTIC ACID, DL-; PHOSPHORIC ACID; POTASSIUM DICHROMATE; TOXICODENDRON PUBESCENS LEAF; URIC ACID
- Active strength
- 30 [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_X]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43689-0003-2 | 43689000302 | 1 BOTTLE in 1 CARTON (43689-0003-2) > 125 mg in 1 BOTTLE (43689-0003-1) | 1 bottle | 2012-10-11 | 2023-01-14 | No | No | Current |