FDA.reportPublic FDA data

MEB Puri-vega

Product NDC
81488-013
11-digit product format
814880013
Labeler code
81488
Product ID
81488-013_04a53245-9a12-49fa-e063-6394a90af203
Type
HUMAN OTC DRUG
Nonproprietary name
MEB Puri-Vega
Dosage form
LIQUID
Route
ORAL
Labeler
Kadesh Incoporation Co,Ltd
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-08-22
Substance
CALCIUM FLUORIDE; FERROSOFERRIC PHOSPHATE; MAGNESIUM CHLORIDE; MAGNESIUM SULFATE HEPTAHYDRATE; SILICON DIOXIDE; SODIUM NITRATE; SULFUR; ZINC
Active strength
6; 7; 7; 7; 4; 5; 4; 8 [hp_X]/300mL; [hp_X]/300mL; [hp_X]/300mL; [hp_X]/300mL; [hp_X]/300mL; [hp_X]/300mL; [hp_X]/300mL; [hp_X]/300mL
Pharmacologic classes
Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
MEB Puri-vega
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CALCIUM FLUORIDE6 [hp_X]/300mL
MAGNESIUM SULFATE HEPTAHYDRATE7 [hp_X]/300mL
SODIUM NITRATE7 [hp_X]/300mL
ZINC7 [hp_X]/300mL
FERROSOFERRIC PHOSPHATE4 [hp_X]/300mL
MAGNESIUM CHLORIDE5 [hp_X]/300mL
SILICON DIOXIDE4 [hp_X]/300mL
SULFUR8 [hp_X]/300mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 8 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
O3B55K4YKIInternal UNII lookup
SK47B8698TInternal UNII lookup
8M4L3H2ZVZInternal UNII lookup
J41CSQ7QDSInternal UNII lookup
91GQH8I5F7Internal UNII lookup
02F3473H9OInternal UNII lookup
ETJ7Z6XBU4Internal UNII lookup
70FD1KFU70Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
03865989-3034-10fc-e063-6394a90ac80bAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
95250459-30e4-45c1-b08a-993044f49109Product name220250805
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
910c1bd7-67d1-44c7-ad4f-9445f827edccProduct name120230808
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
e7e58cd3-cacb-49df-8d34-1ee335614abbProduct name120150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81488-013-03MEB Puri-vega300 mL in 1 BOTTLELIQUID3002
81488-013-10MEB Puri-vega1000 mL in 1 BOTTLELIQUID10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81488-013MEB PURI-VEGA LIQUID [KADESH INCOPORATION CO,LTD]2Current NDC, 2 package rows20230906_03865989-3034-10fc-e063-6394a90ac80b.zip

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
MEB Puri-vegaMEB PURI-VEGAKadesh Incoporation Co,Ltd03865989-3034-10fc-e063-6394a90ac80b2023-09-05WarningsExact identifier
ndc (product): 81488-013

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
81488-013-0381488001303300 mL in 1 BOTTLE (81488-013-03) 300 ml2023-08-22NoNoCurrent
81488-013-10814880013101000 mL in 1 BOTTLE (81488-013-10) 1000 ml2023-08-22NoNoCurrent