0.9% SODIUM CHLORIDE IRRIGATION

Manufacturer
AMCO INTERNATIONAL CORP
Effective date
2024-12-16
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 21:19:35

Label at a glance#

Product0.9% SODIUM CHLORIDE IRRIGATION
Active ingredientSODIUM CHLORIDE
Label structure4 sections

Label contents#

Full prescribing information#

INSTRUCTIONS FOR USE SECTION

Directions for Use of Flexible Plastic Irrigation Containers

If desired, warm in overwrap to near body temperature in a water bath or oven heated to not more than 45°C. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permit.

DIRECTIONS FOR USE

Tear overwrap down side at slit and remove solution container. Visually inspect the container. If the outlet port protector is damaged, detached, or not present, discard container as solution path sterility may be impaired. Some opacity of the plastic due to moisture absorption during the sterilization process may be observed. This is normal and does not affect the solution quality or safety. The opacity will diminish gradually. Check for minute leaks by squeezing bag firmly. If leaks are found, discard solution as sterility may be impaired. Use Aseptic Technique. 1.Suspend container using hanger hole. 2.Remove plastic protector from outlet port at bottom of container 3.Attach irrigation set. Refer to complete directions accompanying set. Exposure of pharmaceutical products to heat should be minimized. Avoid excessive heat. It is recommended the product be stored at room temperature (25°C): brief exposure up to 40°C does not adversely affect the product

HEALTH CARE PROVIDER LETTER SECTION

Dear Healthcare Professional,
To prevent a drug shortage of large volume parenteral fluid drug products, we plan
to coordinate with the U.S. Food and Drug Administration (FDA) to temporarily import 0.9% Sodium Chloride IRRIGATION ( 3,000 mL) from specific DRE
manufacturing facilities. FDA has not approved these products manufactured by this facility. We are also working to label and produce this drug domestically in the United States.
You may be provided with additional letters for other imported products you receive. Please read each letter in its entirety because each letter may contain different product specific information.
All labels are in English with NDC listed on label.
It is important to note the following:

After opening the carton or box, the bags should be inspected visually to confirm there is no visible particulate matter or bag defects, such as leaks. Container integrity is imperative to ensure sterility of products. Parenteral drug products should be inspected visually for particulate matter and bag defects prior to administration, whenever solution or container permits.

USE A NEW BAG IF PARTICULATES ARE VISIBLE OR IF THE IV BAG CONTAINS A LEAK.
Reporting Adverse Events or Product Quality Issues
To report adverse events associated with these imported products, please call AMCO at+1 833 3 MY AMCO.
. Adverse events or quality problems experienced with the use of these imported products may also be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax

• Complete and submit the report Online: www.fda.gov/medwatch/report.htm
• Regular mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call

1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178 (1-800-332-0178).
To report product quality issues associated with these imported products, please contact AMCO at +1 833 3 MY AMCO.
If you have any questions about the information contained in this letter or the use of the imported products, please Contact +1 833 3 MY AMCO.
To place an order, please contact AMCO at +1 833 3 MY AMCO.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3000 mL NDC NOT FOR INJECTION 0.9% SODIUM CHLORIDE Irrigation USP Each 100 mL contains 900 mg Sodium Chloride USP No antimicrobial agent has been added pH 5.5 (4.5 to 7.0) mEq/L Sodium 154 Chloride 154 Osmolarity 308 mOsmol/L (calc) Sterile Nonpyrogenic Single dose container Do not use unless solution is clear Discard unused portion Cautions Squeeze and inspect inner bag which maintains product sterility Discard if leaks are found Rx Only Store unit in moisture barrier overwrap at room temperature (25°C) until ready to use Avoid excessive heat See insert 0.9% Sodium Chloride NaCl Irrigation USP

LABELLABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CARTON LABELCARTON LABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
486515sodium chloride 0.9 % Irrigation SolutionPSN1
486515sodium chloride 0.154 MEQ/ML Irrigation SolutionSCD1
486515NaCl 0.154 MEQ/ML Irrigation SolutionSY1
486515sodium chloride 0.9 % Irrigation SolutionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84866-6670-10.9% SODIUM CHLORIDE IRRIGATION3000 mL in 1 BAGIRRIGANT30001
84866-6670-40.9% SODIUM CHLORIDE IRRIGATION10 in 1 CARTONIRRIGANT101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84866-66700.9% SODIUM CHLORIDE IRRIGATION (BLUE PHARMA, TOTALCARE, 0.9% SODIUM CHLORIDE IRRIGATION) IRRIGANT [AMCO INTERNATIONAL CORP]12 package rows20241218_29682ecd-0b01-5e83-e063-6294a90a0e12.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84866-667084866-6670-1, 84866-6670-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM CHLORIDE451W47IQ8XACTIB
WATER059QF0KO0RIACT

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
29682ecd-0b02-5e83-e063-6294a90a0e1229682ecd-0b01-5e83-e063-6294a90a0e122024-12-16Exact identifier
spl id: 29682ecd-0b02-5e83-e063-6294a90a0e12
spl set id: 29682ecd-0b01-5e83-e063-6294a90a0e12

Reported adverse events (FAERS/openFDA)#

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