FDA.reportPublic FDA data

DRY-CID

Manufacturer
Aqua Medica, S.A. de C.V.
Effective date
2025-11-10
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:43:02

Label at a glance#

ProductDRY-CID
Active ingredientPOTASSIUM CHLORATE
Label structure13 sections

Storage and handling

Store at room temperature. Keep container tightly closed when not in use.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

By diluting the contents of this box to complete 20
gal (75.70 l), one part of this acid concentrate with
44 parts of purified water (UNE-EN ISO
23500-3:2019 standard) will have the following
concentrations:
Sodium
Potassiu m
Calcium
Magnesium
chlorides
Acetate
Dextrose
The final conductivity calculated at 25°C It is 13,2 to 14,2 mS/cm
NON STERILE PRODUCT
100,00 mEq/l
2,00 mEq/l
2,50 mEq/l
1,00 mEq/l
105,50 mEq/l
4,00 mEq/l
100,00 mg/dl

OTC - ACTIVE INGREDIENT SECTION

Potassium Chlorate

OTC - PURPOSE SECTION

For use with 3-pump hemodialysis machines only.

INDICATIONS & USAGE SECTION

For use with 3-pump hemodialysis machines only, using purified water (Standard 13959:2014) and in conbination with

WARNINGS SECTION

For use with 3-pump hemodialysis machines only.

OTC - DO NOT USE SECTION

If the warranty seal is damaged or broken and do not allow debris to fall into the concentrate.

OTC - WHEN USING SECTION

Using purified water (Standard 13959:2014) and in conbination with sodium bicarbonate.

OTC - STOP USE SECTION

If you do not use the entire contents, discard the excess.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

By diluting one part of this acid concentrate with 44 parts of purified water (ISO Standard 13959:2014).

STORAGE AND HANDLING SECTION

Store at room temperature.

Keep container tightly closed when not in use.

INACTIVE INGREDIENT SECTION

Sodium Chloride, Anhydrous Calcium Chloride, Anhydrous Magnesium Chloride, Acetic Acid, Dextrosa

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DRY-CID LABELDRY-CID LABEL81943-601-01

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
cb89b86a-369e-4204-8910-ae797c503af3Product name120230706
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
d4880ace-a516-8c47-8dfd-73a4ba5887d7Product name220180830
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
48747306-602a-42cc-957b-5b0c69158eeeProduct name120180604
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
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
db5ebcdb-b6ae-21cd-4dc5-76cd84b5578bProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81943-601-012024-11-18C16284748780-11030e365-0e99-111a-e063-dadaa90a10e20404b5ce-f8a2-74ad-e063-6294a90a0337
81943-601-012024-11-18C16284748780-11030e365-0e99-111a-e063-dadaa90a10e20404b5ce-f8a2-74ad-e063-6294a90a0337
81943-601-012024-07-30C16284748780-11030e365-0e99-111a-e063-dadaa90a10e20404b5ce-f8a2-74ad-e063-6294a90a0337
81943-601-012024-07-30C16284748780-11030e365-0e99-111a-e063-dadaa90a10e20404b5ce-f8a2-74ad-e063-6294a90a0337
81943-601-012024-01-30C16284748780-11030e365-0e99-111a-e063-dadaa90a10e20404b5ce-f8a2-74ad-e063-6294a90a0337
81943-601-012024-01-30C16284748780-11030e365-0e99-111a-e063-dadaa90a10e20404b5ce-f8a2-74ad-e063-6294a90a0337

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81943-601-01DRY-CID25.28 kg in 1 BOXPOWDER, FOR SOLUTION25.283

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81943-60181943-601-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM CHLORIDE451W47IQ8XIACT
POTASSIUM CHLORATEH35KS68EE7ACTIB
CALCIUM CHLORIDE ANHYDROUSOFM21057LPIACT
MAGNESIUM CHLORIDE ANHYDROUS59XN63C8VMIACT
ACETIC ACIDQ40Q9N063PIACT
ANHYDROUS DEXTROSE5SL0G7R0OKIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22024-11-18full-release2026-06-01 00:37:43

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
DRY-CIDDRY CONCENTRATE FOR HEMODIALYSISAqua Medica, S.A. de C.V.0404b5ce-f8a2-74ad-e063-6294a90a03372025-11-10WarningsExact identifier
ndc (package): 81943-601-01
ndc (product): 81943-601
ndc11 (package): 81943060101
spl id: 43486b30-74af-3034-e063-6394a90a2e1e
spl set id: 0404b5ce-f8a2-74ad-e063-6294a90a0337

Reported adverse events (FAERS/openFDA)#

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