ACD-A- anticoagulant citrate dextrose solution formula a solution 
Fenwal, Inc.

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Anticoagulant Citrate Dextrose Solution USP (ACD) Formula A

CAUTION —

DO NOT REMOVE UNIT FROM OVERWRAP UNTIL READY FOR USE

THE OVERWRAP IS A MOISTURE BARRIER
THE INNER BAG MAINTAINS THE STERILITY OF THE PRODUCT

RECOMMENDED STORAGE–STORE AT CONTROLLED ROOM TEMPERATURE.

CODE 4B7891X
NDC 0942-0641-04

1000 mL

Fenwal™

Anticoagulant Citrate Dextrose Solution USP (ACD) Formula A

EACH 100 mL CONTAINS 2.45 g DEXTROSE (MONOHYDRATE) USP 2.2 g SODIUM CITRATE (DIHYDRATE) USP 730 mg CITRIC ACID (ANHYDROUS) USP

STERILE

NONPYROGENIC

SINGLE USE CONTAINER

DISCARD UNUSED PORTION

FOR USE WITH CYTAPHERESIS DEVICE ONLY

NOT FOR DIRECT INTRAVENOUS INFUSION

DO NOT USE UNLESS SOLUTION IS CLEAR AND NO LEAKS ARE DETECTED

AFTER REMOVING OVERWRAP CHECK FOR MINUTE LEAKS BY SQUEEZING INNER BAG FIRMLY. IF LEAKS ARE FOUND DISCARD SOLUTION AS STERILITY MAY BE IMPAIRED

Rx only

PL 146 PLASTIC

Manufactured by:
Baxter Healthcare Corporation
Deerfield, IL 60015 USA

logoManufactured for:
Fenwal, Inc.
Lake Zurich, IL 60047 USA

07-25-58-006         Made in USA

LABEL ISSUE DATE    05/2008

PACKAGE/LABEL DISPLAY PANEL

Anticoagulant Citrate Dextrose Solution USP (ACD) Formula A label
ACD-A 
anticoagulant citrate dextrose solution formula a solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0942-0641
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Dextrose Monohydrate (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) Dextrose Monohydrate24.5 g  in 1000 mL
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) (Anhydrous Citric Acid - UNII:XF417D3PSL) SODIUM CITRATE, UNSPECIFIED FORM22 g  in 1000 mL
Anhydrous Citric Acid (UNII: XF417D3PSL) (Anhydrous Citric Acid - UNII:XF417D3PSL) Anhydrous Citric Acid7.3 g  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0942-0641-041000 mL in 1 BAG; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDABN16091803/01/2007
Labeler - Fenwal, Inc. (794519020)
Registrant - Fenwal, Inc. (794519020)
Establishment
NameAddressID/FEIBusiness Operations
Baxter Healthcare Corporation059140764MANUFACTURE(0942-0641)

Revised: 2/2022
Document Id: 052fbb41-5092-4bdb-a356-cbf27ce5bf23
Set id: ab19b011-0a51-4f04-9881-d9fc7cae95ae
Version: 6
Effective Time: 20220211
 
Fenwal, Inc.