FDA.reportPublic FDA data

Gout Symptom Relief

Product NDC
57955-9975
11-digit product format
579559975
Labeler code
57955
Product ID
57955-9975_4590e343-960e-4fa7-888e-8b9ed5ad93bd
Type
HUMAN OTC DRUG
Nonproprietary name
Ammon phos, Belladonna, Colchicum autumnale, Formicum acidum, Fraxinus excelsior, Ledum palustre, Natrum carbonicum, Nux vomica and Urtica urens.
Dosage form
LIQUID
Route
ORAL
Labeler
King Bio Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2026-03-10
Substance
AMMONIUM PHOSPHATE, DIBASIC; ATROPA BELLADONNA; COLCHICUM AUTUMNALE BULB; FORMIC ACID; FRAXINUS EXCELSIOR BARK; FRAXINUS EXCELSIOR LEAF; RHODODENDRON TOMENTOSUM LEAFY TWIG; SODIUM CARBONATE; STRYCHNOS NUX-VOMICA SEED; URTICA URENS WHOLE
Active strength
10; 10; 10; 10; 10; 10; 10; 10; 10; 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
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Gout Symptom Relief
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AMMONIUM PHOSPHATE, DIBASIC10 [hp_X]/59mL
ATROPA BELLADONNA10 [hp_X]/59mL
COLCHICUM AUTUMNALE BULB10 [hp_X]/59mL
FORMIC ACID10 [hp_X]/59mL
FRAXINUS EXCELSIOR BARK10 [hp_X]/59mL
FRAXINUS EXCELSIOR LEAF10 [hp_X]/59mL
RHODODENDRON TOMENTOSUM LEAFY TWIG10 [hp_X]/59mL
SODIUM CARBONATE10 [hp_X]/59mL
STRYCHNOS NUX-VOMICA SEED10 [hp_X]/59mL
URTICA URENS WHOLE10 [hp_X]/59mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii10LGE70FSU, WQZ3G9PF0H, 993QHL78E6, 0YIW783RG1, R6KCX5H8I2, RC38362Q7M, 877L01IZ0P, 45P3261C7T, 269XH13919, IHN2NQ5OF9

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-9975-2Gout Symptom Relief59 mL in 1 BOTTLE, SPRAYLIQUID591

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
57955-9975-25795599750259 mL in 1 BOTTLE, SPRAY (57955-9975-2) 59 ml2026-03-10NoNoCurrent