Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Chronagesic NDC 43742-2207
Alpha lipoic acid 8 [hp_X]/mL + 17 more ingredients · Liquid · Oral · Deseret Biologicals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 43742-2207-1 | 43742220701 | 30 mL in 1 BOTTLE, DROPPER (43742-2207-1)Marketed from Nov 8, 2024 |
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)
- alpha-lipoicum acidum, apiolum, arnica montana, cartilago suis, cinnamomum, dulcamara, funiculus umbilicalis suis, nadidum, natrum oxalaceticum, pantothenic acid, placenta totalis suis, piper nigrum, rhus tox, sanguinaria canadensis, sulphur, silicea, symphytum officinale, thuja occidentalis
- Active ingredients
- Alpha lipoic acid — 8 [hp_X]/mLApiole (Parsley) — 16 [hp_C]/mLArnica montana whole — 3 [hp_X]/mLSus scrofa cartilage — 8 [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]/mLGreen peppercorn — 6 [hp_X]/mLToxicodendron pubescens leaf — 8 [hp_X]/mLSanguinaria canadensis root — 6 [hp_X]/mLSulfur — 6 [hp_X]/mLSilicon dioxide — 8 [hp_X]/mLComfrey root — 8 [hp_X]/mLThuja occidentalis leafy twig — 12 [hp_X]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Deseret Biologicals, Inc.
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- 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 43742-2207_0f5d014c-1ff1-406a-a1a0-5a04d055b766SPL ID 0f5d014c-1ff1-406a-a1a0-5a04d055b766SPL set ID 1e340282-dbd9-44d7-9924-807f4099cf0cUNII 73Y7P0K73Y, QQ67504PXO, O80TY208ZW, 73ECW5WG2F, 5S29HWU6QB, KPS1B1162N, 118OYG6W3H, 0U46U6E8UK, 6CA025Y4FG, 19F5HK2737, C8CV8867O8, 6G53L8ESRK, 6IO182RP7A, N9288CD508, 70FD1KFU70, ETJ7Z6XBU4, M9VVZ08EKQ, 1NT28V9397UPC 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
N443742220701followed by a unit qualifier and the quantityPackage 43742-2207-01. 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.