Unique Pain Reduction Arthritis
- Product NDC
- 50845-0184
- 11-digit product format
- 508450184
- Labeler code
- 50845
- Product ID
- 50845-0184_d3e91485-41bc-46f1-93e5-e375ccb77b98
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum Napellus, Apis Mellifica, Benzoicum Acidum, Cartilago Suis, Colchicum Autumnale, Eupatorium Perfoliatum, Guaiacum, Hypericum Perforatum, Ledum Palustre, Mercurius Corrosivus, Rhus Tox, Thuja Occidentalis
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Liddell Laboratories, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-12-10
- Marketing end
- 2022-01-07
- Substance
- ACONITUM NAPELLUS; APIS MELLIFERA; BENZOIC ACID; SUS SCROFA CARTILAGE; COLCHICUM AUTUMNALE BULB; EUPATORIUM PERFOLIATUM FLOWERING TOP; GUAIACUM OFFICINALE RESIN; HYPERICUM PERFORATUM; LEDUM PALUSTRE TWIG; MERCURIC CHLORIDE; TOXICODENDRON PUBESCENS LEAF; THUJA OCCIDENTALIS LEAFY TWIG
- Active strength
- 200 [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
- 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 |
|---|
| 50845-0184-1 | 50845018401 | 30 mL in 1 BOTTLE, DROPPER (50845-0184-1) | 30 ml | 2015-12-10 | 2022-01-07 | No | No | Current |