Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Guna-Stomach NDC 17089-302
Picea mariana resin 3 [hp_X]/4g + 14 more ingredients · Pellet · Oral · Guna spa
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 17089-302-20 | 17089030220 | 2 TUBE in 1 BOX (17089-302-20) / 4 g in 1 TUBEMarketed from May 15, 2018 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
- Guna-Stomach
- Generic name (nonproprietary)
- activated charcoal - antimony trisulfide - bismuth subnitrate - dioscorea villosa root - dopamine - human epidermal growth factor - ipecac - oregano - picea mariana resin - robinia pseudoacacia bark - semecarpus anacardium juice - silver nitrate - sus scrofa stomach - sus scrofa sympathetic nerve - momordica balsamina immature fruit -
- Active ingredients
- Picea mariana resin — 3 [hp_X]/4gSemecarpus anacardium juice — 30 [hp_X]/4gAntimony trisulfide — 30 [hp_X]/4gSilver nitrate — 30 [hp_X]/4gBismuth subnitrate — 6 [hp_X]/4gActivated charcoal — 6 [hp_X]/4gIpecac — 30 [hp_X]/4gDioscorea villosa root — 3 [hp_X]/4gDopamine — 6 [hp_X]/4gHuman epidermal growth factor — 4 [hp_C]/4gMomordica balsamina immature fruit — 3 [hp_X]/4gOregano — 10 [hp_X]/4gRobinia pseudoacacia bark — 2 [hp_X]/4gSus scrofa stomach — 30 [hp_X]/4gSus scrofa sympathetic nerve — 6 [hp_X]/4g
- Dosage form
- Pellet
- Route
- Oral
- Labeler
- Guna spa
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Other FDA classes
- Allergens (Chemical structure)Bismuth (Chemical structure)Catecholamines (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)
- Identifiers
- Product ID 17089-302_ed80d394-0e03-88a4-e053-2995a90a6b2bSPL ID ed80d394-0e03-88a4-e053-2995a90a6b2bSPL set ID 7805055c-e5f6-4d1d-9449-a5dce8a066ebUNII 71AOV0W131, Y0F0BU8RDU, F79059A38U, 95IT3W8JZE, H19J064BA5, 2P3VWU3H10, 62I3C8233L, IWY3IWX2G8, VTD58H1Z2X, TZK30RF92W, WUW1665V10, 0E5AT8T16U, 7TPC058OWY, T0920P9Z9A, H6L0IFR3FE
- Pharmacologic class
- Bismuth; Catecholamine; 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
N417089030220followed by a unit qualifier and the quantityPackage 17089-0302-20. 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)
DIRECTIONS Turn tube upside down and rotate cap to release pellets into cap. Unscrew cap and without touching pellets tip them into the mouth under the tongue. Allow to dissolve Take 15 minutes before meals.
Excerpt only. Read the full label for complete information.