Goutinex
- Product NDC
- 49726-023
- 11-digit product format
- 497260023
- Labeler code
- 49726
- Product ID
- 49726-023_7df183c1-5f62-1a16-e053-2991aa0a2223
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACTAEA SPICATA, AMMONIUM PHOSPHORICUM, BELLADONNA, COLCHICUM AUTUMNALE, FORMICUM ACIDUM, FRAXINUS EXCELSIOR, LEDUM PALUSTRE, NATRUM CARBONICUM, NUX VOMICA, PHYTOLACCA DECANDRA, RHODODENDRON CHRYSANTHUM, SALICYLICUM ACIDUM, URTICA URENS
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Hello Life, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2011-11-09
- Marketing end
- 0000-00-00
- Substance
- 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
- Active strength
- 10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| efd58dcf-540a-4531-8766-e713129ca6f2 | Product name | 1 | 20250307 |
| 4b7700e3-6e0e-45e5-9d22-6f754d61386e | Product name | 2 | 20250304 |
| 726062af-1135-4707-a1d7-57256991bbf9 | Product name | 2 | 20250226 |
| dea2eded-d1e7-46bb-9a3d-f8dc20de6277 | Product name | 1 | 20190408 |
| 7cda52fc-125f-421c-8fea-bc1974370c49 | Product name | 2 | 20180703 |
| 0ca1d589-929b-4b33-bc5b-1d84abdafa6a | Product name | 1 | 20150324 |
| fc363c46-397b-4476-ac0f-70e43e8e4592 | Product name | 1 | 20150324 |
| 19c71a3d-ed9c-166b-a7e5-38c250c35631 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 49726-023-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-23ca-f424-e053-dadaa90a57ce | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49726-023-02 | GoutinexGout Symptom Relief | 59 mL in 1 BOTTLE, DROPPER | LIQUID | 59 | 10 | |
| 49726-023-02 | GoutinexGout Symptom Relief | 1 in 1 CARTON | LIQUID | 1 | 10 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 49726-023 | GOUTINEX GOUT SYMPTOM RELIEF (ACTAEA SPICATA, AMMONIUM PHOSPHORICUM, BELLADONNA, COLCHICUM AUTUMNALE, FORMICUM ACIDUM, FRAXINUS EXCELSIOR, LEDUM PALUSTRE, NATRUM CARBONICUM, NUX VOMICA, PHYTOLACCA DECANDRA, RHODODENDRON CHRYSANTHUM, SALICYLICUM ACIDUM, URTICA URENS) LIQUID [HELLO LIFE, INC.] | 10 | Legacy NDC, 2 package rows | 20181227_4243e27f-ce96-4e73-9948-be88c5d02726.zip |
Packages#
| Package NDC | 11-digit format | Description | Units | Status |
|---|---|---|---|---|
| 49726-023-02 | 49726002302 | 59 mL in 1 BOTTLE, DROPPER | 59 ml | Historical |