49726-023 : Goutinex Oral Liquid
| NDC: | 49726-023 |
| Labeler: | Ionx Holdings D/B/A Hellolife Inc. |
| Product Type: | Human OTC Drug |
| Drug Name: | Goutinex Gout Symptom Relief |
| Dosage Form: | Oral Liquid |
| Rev. Date: |
NDC Package Codes:
- 49726-023-02: 59 ML IN 1 BOTTLE, DROPPER (49726‑023‑02)
Active Ingredients:
- Actaea Spicata Root
- Ammonium Phosphate
- Dibasic
- Atropa Belladonna
- Colchicum Autumnale Bulb
- Formic Acid
- Sodium Carbonate
- Strychnos Nux-vomica Seed
- Phytolacca Americana Root
- Rhododendron Aureum Leaf
- Salicylic Acid
- Urtica Urens
- Ledum Palustre Twig
- Fraxinus Excelsior Leaf
Dosage Strength:
- 10 [hp_X]/59mL
- 10 [hp_X]/59mL
- 10 [hp_X]/59mL
- 10 [hp_X]/59mL
- 10 [hp_X]/59mL
- 10 [hp_X]/59mL
- 10 [hp_X]/59mL
- 10 [hp_X]/59mL
- 10 [hp_X]/59mL
- 10 [hp_X]/59mL
- 10 [hp_X]/59mL
- 10 [hp_X]/59mL
- 10 [hp_X]/59mL
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.
