DRY-CID- dry concentrate for hemodialysis powder, for solution

DRY-CID by

Drug Labeling and Warnings

DRY-CID by is a Otc medication manufactured, distributed, or labeled by Aqua Medica, S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

ACTIVE INGREDIENT

Potassium Chlorate

PURPOSE

For use with 3-pump hemodialysis machines only.

INDICATIONS & USAGE

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

WARNINGS

For use with 3-pump hemodialysis machines only.

DO NOT USE

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

WHEN USING

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

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

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

STORAGE AND HANDLING

Store at room temperature.

Keep container tightly closed when not in use.

INACTIVE INGREDIENT

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

PRINCIPAL DISPLAY PANEL

81943-601-01

INGREDIENTS AND APPEARANCE

DRY-CID 
dry concentrate for hemodialysis powder, for solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81943-601
Route of Administration	HEMODIALYSIS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POTASSIUM CHLORATE (UNII: H35KS68EE7) (CHLORATE ION - UNII:08Z8093742)	POTASSIUM CHLORATE	0.51 kg  in 100 kg

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	19.91 kg  in 100 kg
CALCIUM CHLORIDE ANHYDROUS (UNII: OFM21057LP)	0.47 kg  in 100 kg
MAGNESIUM CHLORIDE ANHYDROUS (UNII: 59XN63C8VM)	0.16 kg  in 100 kg
ACETIC ACID (UNII: Q40Q9N063P)	0.82 kg  in 100 kg
ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)	3.41 kg  in 100 kg
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81943-601-01	25.28 kg in 1 BOX; Type 0: Not a Combination Product	08/30/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/30/2023

Labeler - Aqua Medica, S.A. de C.V. (589696442)

Establishment
Name	Address	ID/FEI	Business Operations
Aqua Medica, S.A. de C.V.		589696442	manufacture(81943-601)