17089-406 : Guna-reflux Oral Solution/ Drops
| NDC: | 17089-406 |
| Labeler: | Guna Spa |
| Product Type: | Human OTC Drug |
| Drug Name: | Guna-reflux |
| Dosage Form: | Oral Solution/ Drops |
| Rev. Date: |
NDC Package Codes:
- 17089-406-18: 1 BOTTLE, DROPPER IN 1 BOX (17089‑406‑18) > 30 ML IN 1 BOTTLE, DROPPER
Active Ingredients:
- Activated Charcoal
- Aethusa Cynapium
- Apomorphine Hydrochloride
- Bryonia Alba Root
- Colchicum Autumnale Bulb
- Ipecac
- Lycopodium Clavatum Spore
- Strychnos Ignatii Seed
- Strychnos Nux-vomica Seed
- Sus Scrofa Esophagus
- Sus Scrofa Stomach
- Watermelon
Dosage Strength:
- 12 [hp_X]/30mL
- 4 [hp_X]/30mL
- 6 [hp_X]/30mL
- 30 [hp_X]/30mL
- 6 [hp_X]/30mL
- 4 [hp_X]/30mL
- 5 [hp_X]/30mL
- 6 [hp_X]/30mL
- 4 [hp_X]/30mL
- 10 [hp_X]/30mL
- 10 [hp_X]/30mL
- 30 [hp_X]/30mL
Pharmaceutical Classes:
- Allergens [CS]
- Allergens [CS]
- Cell-mediated Immunity [PE]
- Dietary Proteins [CS]
- Dopamine Agonists [MoA]
- Dopaminergic Agonist [EPC]
- Fruit Proteins [EXT]
- Increased Histamine Release [PE]
- Increased IgG Production [PE]
- Non-Standardized Food Allergenic Extract [EPC]
- Non-Standardized Plant Allergenic Extract [EPC]
- Plant Proteins [CS]
- Seed Storage Proteins [CS]
NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.
