FDA.reportPublic FDA data

Uric Acid Combination

Product NDC
63083-9307
11-digit product format
630839307
Labeler code
63083
Product ID
63083-9307_f1791c2d-4b6a-4f62-9eec-defc383f3475
Type
HUMAN OTC DRUG
Nonproprietary name
Uric Acid Combination
Dosage form
LIQUID
Route
ORAL
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1984-08-15
Substance
1,3-BIS(BENZOTHIAZOL-2-YLTHIOMETHYL)UREA; COLCHICUM AUTUMNALE BULB; FERROSOFERRIC PHOSPHATE; GLUTAMINE; LITHIUM CARBONATE; SODIUM CARBONATE; STRYCHNOS NUX-VOMICA SEED; TOXICODENDRON PUBESCENS LEAF; URIC ACID
Active strength
12; 4; 8; 12; 8; 3; 6; 6; 12 [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL
Pharmacologic classes
Allergens [CS], Amino Acid [EPC], Amino Acids [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Mood Stabilizer [EPC], 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
Uric Acid Combination
Brand name suffix
9307
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
1,3-BIS(BENZOTHIAZOL-2-YLTHIOMETHYL)UREA12 [hp_X]/29.5mL
COLCHICUM AUTUMNALE BULB4 [hp_X]/29.5mL
FERROSOFERRIC PHOSPHATE8 [hp_X]/29.5mL
GLUTAMINE12 [hp_X]/29.5mL
LITHIUM CARBONATE8 [hp_X]/29.5mL
SODIUM CARBONATE3 [hp_X]/29.5mL
STRYCHNOS NUX-VOMICA SEED6 [hp_X]/29.5mL
TOXICODENDRON PUBESCENS LEAF6 [hp_X]/29.5mL
URIC ACID12 [hp_X]/29.5mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii0214C2T14J, 993QHL78E6, 91GQH8I5F7, 0RH81L854J, 2BMD2GNA4V, 45P3261C7T, 269XH13919, 6IO182RP7A, 268B43MJ25

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
73df98bc-429f-4587-8299-6ad8d52a4f36Product name220250304
b3053bb1-353b-4a0b-bca5-28fe7228957cProduct name220250124
8ce6e144-236f-b7be-f690-f06e0c8c6bd3Product name220170725
f09af6ee-c6dd-d0ce-77ad-93508bcdacedProduct name420161205
64b87b8d-6ae7-cef1-8fd2-34228b0cc1bcProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-9307-12026-01-09C16284748780-11030e365-2020-111a-e063-dadaa90a10e2R307
63083-9307-12026-01-09C16284748780-11030e365-2020-111a-e063-dadaa90a10e2R307
63083-9307-12024-01-30C16284748780-11030e365-2020-111a-e063-dadaa90a10e2R307
63083-9307-12024-01-30C16284748780-11030e365-2020-111a-e063-dadaa90a10e2R307

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-9307-1Uric Acid Combination930729.5 mL in 1 BOTTLE, DROPPERLIQUID29.52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-9307URIC ACID COMBINATION 9307 (URIC ACID COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Current NDC, Legacy NDC, 1 package rows20220211_3f136f86-a9ed-4a04-98cb-81abe33cd181.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-9307-16308393070129.5 mL in 1 BOTTLE, DROPPER (63083-9307-1) 29.5 ml1985-08-150000-00-00NoNoCurrent