Prescription drug · UNAPPROVED HOMEOPATHIC
Chronagesic NDC 43742-1665
Arnica montana whole 3 [hp_X]/mL + 17 more ingredients · Liquid · Oral · Deseret Biologicals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 43742-1665-1 | 43742166501 | 30 mL in 1 BOTTLE, DROPPER (43742-1665-1)Marketed from Jun 15, 2020 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Chronagesic
- Generic name (nonproprietary)
- arnica montana, cinnamomum, dulcamara, funiculus umbilicalis suis, nadidum, natrum oxalaceticum, pantothenic acid, placenta totalis suis, sanguinaria canadensis, sulphur, piper nigrum, alpha-lipoicum acidum, cartilago suis, rhus tox, silicea, symphytum officinale, thuja occidentalis, apiolum
- Active ingredients
- Arnica montana whole — 3 [hp_X]/mLCinnamon — 6 [hp_X]/mLSolanum dulcamara top — 6 [hp_X]/mLSus scrofa umbilical cord — 6 [hp_X]/mLNadide — 6 [hp_X]/mLSodium diethyl oxalacetate — 6 [hp_X]/mLPantothenic acid — 6 [hp_X]/mLSus scrofa placenta — 6 [hp_X]/mLSanguinaria canadensis root — 6 [hp_X]/mLSulfur — 6 [hp_X]/mLGreen peppercorn — 6 [hp_X]/mLAlpha lipoic acid — 8 [hp_X]/mLSus scrofa cartilage — 8 [hp_X]/mLToxicodendron pubescens leaf — 8 [hp_X]/mLSilicon dioxide — 8 [hp_X]/mLComfrey root — 8 [hp_X]/mLThuja occidentalis leafy twig — 12 [hp_X]/mLApiole (Parsley) — 16 [hp_C]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Deseret Biologicals, Inc.
- Product type
- Prescription drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Marketing end
- Other FDA classes
- Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)
- Identifiers
- Product ID 43742-1665_446da5cc-e452-4416-a9c4-0788ddc3106bSPL ID 446da5cc-e452-4416-a9c4-0788ddc3106bSPL set ID 66e351ed-d359-4367-a950-fc57b37489abUNII O80TY208ZW, 5S29HWU6QB, KPS1B1162N, 118OYG6W3H, 0U46U6E8UK, 6CA025Y4FG, 19F5HK2737, C8CV8867O8, N9288CD508, 70FD1KFU70, 6G53L8ESRK, 73Y7P0K73Y, 73ECW5WG2F, 6IO182RP7A, ETJ7Z6XBU4, M9VVZ08EKQ, 1NT28V9397, QQ67504PXOUPC 0810151880952
- Pharmacologic class
- Non-Standardized Food Allergenic Extract
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N443742166501followed by a unit qualifier and the quantityPackage 43742-1665-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
USES: • For the temporary relief of symptoms including: • joint support • joint pain • joint stiffness These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Excerpt only. Read the full label for complete information.