FDA.reportPublic FDA data

kumary

Manufacturer
METAZONKEY LLC
Effective date
2024-11-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:34:03

Label at a glance#

Productkumary
Active ingredientCHONDROITIN SULFATE (BOVINE), HYDROLYZED SHEEP WOOL KERATIN (200 MW), HYALURONIC ACID, CALCIUM CARBONATE, TURMERIC, COLLAGEN ALPHA-2(I) CHAIN BOVINE, MAGNESIUM OXIDE, POVIDONE-IODINE, MAGNESIUM STEARATE, ASCORBIC ACID
Label structure7 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

For adults take 1 tablet with water dailyFor adults take 1 tablet with water dailyFor adults take 1 tablet with water daily

WARNINGS SECTION

WARNINGWARNING WARNING: If you are pregnant, nursing, taking any medicationsor planning any medical procedure, consult your physician before use. Discontinue use and consult your physician if any adverse reactions occour. Keep out of reach of children.
Store in dry place under controlled room temperature: 20 - 25 °C
(68-77°F)

INACTIVE INGREDIENT SECTION

SUPPLEMENT FACTSSUPPLEMENT FACTS

INDICATIONS & USAGE SECTION

indicationsindications

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keepkeep

OTC - PURPOSE SECTION

purposepurpose

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

K-umaryK-umary

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ASCORBIC ACID Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
CALCIUM CATION Pharmacologic Class Indexing3Indexing - Pharmacologic Class20230427
MAGNESIUM CATION Pharmacologic Class Indexing4Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
95250459-30e4-45c1-b08a-993044f49109Product name220250805
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
e7e58cd3-cacb-49df-8d34-1ee335614abbProduct name120150609
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84858-1010-12026-01-29C16284748780-149896155-bba6-586f-e063-e6dba90add9025e0786b-ed1d-ad45-e063-6294a90a01c5
84858-1010-22026-01-29C16284748780-149896155-bba6-586f-e063-e6dba90add9025e0786b-ed1d-ad45-e063-6294a90a01c5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84858-1010-1kumary30 U in 1 BOTTLE, PLASTICTABLET302
84858-1010-2kumary30 U in 1 BOTTLE, PLASTICTABLET302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84858-1010KUMARY (K-UMARY) TABLET [METAZONKEY LLC]22 package rows20241106_25e0786b-ed1d-ad45-e063-6294a90a01c5.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84858-101084858-1010-1, 84858-1010-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLUCOSAMINE SULFATE1FW7WLR731IACT
CHONDROITIN SULFATE (BOVINE)6IC1M3OG5ZACTIM
HYDROLYZED SHEEP WOOL KERATIN (200 MW)R6K7AW17SUACTIB
HYALURONIC ACIDS270N0TRQYACTIB
CALCIUM CARBONATEH0G9379FGKACTIM
TURMERIC856YO1Z64FACTIB
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
COLLAGEN ALPHA-2(I) CHAIN BOVINEYRU8Z30SXIACTIB
MAGNESIUM OXIDE3A3U0GI71GACTIB
POVIDONE-IODINE85H0HZU99MACTIM
CELLULOSE, MICROCRYSTALLINEOP1R32D61UIACT
MAGNESIUM STEARATE70097M6I30ACTIB
ASCORBIC ACIDPQ6CK8PD0RACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
262ccab2-703a-27a7-e063-6394a90a919325e0786b-ed1d-ad45-e063-6294a90a01c52024-11-05WarningsExact identifier
spl id: 262ccab2-703a-27a7-e063-6394a90a9193
spl set id: 25e0786b-ed1d-ad45-e063-6294a90a01c5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.