Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Amoe Combination NDC 43742-1681
Baptisia tinctoria root 3 [hp_X]/mL + 21 more ingredients · Liquid · Oral · Deseret Biologicals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 43742-1681-1 | 4374216810143742168101 | 30 mL in 1 BOTTLE, DROPPER (43742-1681-1)Marketed from May 14, 2021 |
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)
- Amoe Combination
- Generic name (nonproprietary)
- baptisia tinctoria, cajuputum, capsicum annuum, fragaria vesca, hamamelis virginiana, quassia (amara), senna (cassia angustifolia), hydrastis canadensis, hepar suis, pancreas suis, spleen (suis), cinchona officinalis, iridium metallicum, lycopodium clavatum, nitricum acidum, nux vomica, selenium metallicum, blastocystis hominis, cryptosporidium parvum, giardia lamblia, entamoeba histolytica, brugia malayi
- Active ingredients
- Baptisia tinctoria root — 3 [hp_X]/mLCajuput oil — 3 [hp_X]/mLCapsicum — 3 [hp_X]/mLFragaria vesca fruit — 3 [hp_X]/mLHamamelis virginiana root bark/stem bark — 3 [hp_X]/mLQuassia amara wood — 3 [hp_X]/mLSenna leaf — 3 [hp_X]/mLGoldenseal — 6 [hp_X]/mLPork liver — 8 [hp_X]/mLSus scrofa pancreas — 8 [hp_X]/mLSus scrofa spleen — 8 [hp_X]/mLCinchona officinalis bark — 12 [hp_X]/mLIridium — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLNitric acid — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLSelenium — 12 [hp_X]/mLBlastocystis hominis — 12 [hp_C]/mLCryptosporidium parvum — 12 [hp_C]/mLGiardia lamblia — 12 [hp_C]/mLEntamoeba histolytica — 18 [hp_C]/mLBrugia malayi — 39 [hp_C]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Deseret Biologicals, Inc.NDC labeler code 43742
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Other FDA classes
- Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
- Identifiers
- Product ID 43742-1681_bec8d450-8b08-4dba-8d18-580e914f48a1SPL ID bec8d450-8b08-4dba-8d18-580e914f48a1SPL set ID 419dfc99-a8e8-46fb-8db5-e64e8a726d4aUNII 5EF0HWI5WU, J3TO6BUQ37, 00UK7646FG, CG6IX3GCMU, T7S323PKJS, S5249Q85HW, AK7JF626KX, ZW3Z11D0JV, 6EC706HI7F, 9Y3J3362RY, 92AMN5J79Y, S003A158SB, 44448S9773, C88X29Y479, 411VRN1TV4, 269XH13919, H6241UJ22B, 66KX72J4H6, TGR919EN5P, 89IEJ09R73, 2XC2HJ478W, V1NN02KTF0UPC 0810151880549
- Pharmacologic class
- Non-Standardized Food Allergenic Extract; Non-Standardized Plant 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
N443742168101followed by a unit qualifier and the quantityPackage 43742-1681-01. 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: • weakness • fever • stomach cramps 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.
About NDC 43742-1681
- What is NDC 43742-1681?
- 43742-1681 is the product NDC for Amoe Combination, Baptisia tinctoria root 3 [hp_X]/mL + 21 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Amoe Combination (Baptisia Tinctoria, Cajuputum, Capsicum Annuum, Fragaria Vesca, Hamamelis Virginiana, Quassia (Amara), Senna (Cassia Angustifolia), Hydrastis Canadensis, Hepar Suis, Pancreas Suis, Spleen (Suis), Cinchona Officinalis, Iridium Metallicum, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Selenium Metallicum, Blastocystis Hominis, Cryptosporidium Parvum, Giardia Lamblia, Entamoeba Histolytica, Brugia Malayi).
- What is the active ingredient?
- Baptisia tinctoria root, Cajuput oil, Capsicum, Fragaria vesca fruit, Hamamelis virginiana root bark/stem bark, Quassia amara wood, Senna leaf, Goldenseal, Pork liver, Sus scrofa pancreas, Sus scrofa spleen, Cinchona officinalis bark, Iridium, Lycopodium clavatum spore, Nitric acid, Strychnos nux-vomica seed, Selenium, Blastocystis hominis, Cryptosporidium parvum, Giardia lamblia, Entamoeba histolytica, Brugia malayi.
- Who is the labeler?
- Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Amoe Combination?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.