Home NDC 63323-186-01 NDC 63323-186-01 - Sodium Chloride This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 63323-186
Requested NDC 63323-186-01
Package NDCs from labels 63323-186-00, 63323-186-04, 63323-186-02, 63323-186-01, 63323-186-10, 63323-186-03, 63323-186-20
Manufacturer Fresenius Kabi USA, LLC
Effective date 2025-11-28
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Sodium Chloride - Fresenius Kabi USA, LLC Fresenius Kabi USA, LLC 2025-11-28 HUMAN PRESCRIPTION DRUG LABEL Sodium Chloride - Cardinal Health 107, LLC Cardinal Health 107, LLC 2025-10-29 HUMAN PRESCRIPTION DRUG LABEL 45764F/Revised: November 2020 SODIUM CHLORIDE INJECTION, USP 0.9% Henry Schein, Inc. 2025-08-07 HUMAN PRESCRIPTION DRUG LABEL Sodium Chloride - A-S Medication Solutions A-S Medication Solutions 2023-12-10 HUMAN PRESCRIPTION DRUG LABEL 45764D/Revised: January 2008 SODIUM CHLORIDE INJECTION, USP 0.9% General Injectables and Vaccines, Inc. 2022-12-28 HUMAN PRESCRIPTION DRUG LABEL Sodium Chloride - Fresenius Kabi USA, LLC Fresenius Kabi USA, LLC 2022-02-10 HUMAN PRESCRIPTION DRUG LABEL P-Care X RX PHARMA-PACK, INC. 2020-02-03 HUMAN PRESCRIPTION DRUG LABEL P-Care MG RX PHARMA-PACK, INC. 2020-02-03 HUMAN PRESCRIPTION DRUG LABEL P-Care K80MX RX PHARMA-PACK, INC. 2020-02-03 HUMAN PRESCRIPTION DRUG LABEL P-Care K40MX RX PHARMA-PACK, INC. 2020-02-03 HUMAN PRESCRIPTION DRUG LABEL P-Care M RX PHARMA-PACK, INC. 2020-02-03 HUMAN PRESCRIPTION DRUG LABEL P-Care D40MX RX PHARMA-PACK, INC. 2020-01-31 HUMAN PRESCRIPTION DRUG LABEL P-Care 100MX RX PHARMA-PACK, INC. 2020-01-31 HUMAN PRESCRIPTION DRUG LABEL Sodium Chloride Injection, USP REMEDYREPACK INC. 2018-09-18 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63323-186-01 Sodium Chloride 10 mL in 1 VIAL, SINGLE-DOSE INJECTION 10 9 63323-186-02 Sodium Chloride 25 in 1 TRAY INJECTION 25 9 63323-186-03 Sodium Chloride 20 mL in 1 VIAL, SINGLE-DOSE INJECTION 20 9 63323-186-04 Sodium Chloride 2 mL in 1 VIAL, SINGLE-DOSE INJECTION 2 9 63323-186-10 Sodium Chloride 25 in 1 TRAY INJECTION 25 9 63323-186-20 Sodium Chloride 25 in 1 TRAY INJECTION 25 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63323-186 SODIUM CHLORIDE (SODIUM CHLORIDE) INJECTION [FRESENIUS KABI USA, LLC
] 9 Current NDC, Legacy NDC, 6 package rows 20220215_f62481fd-fcdb-4be6-ac13-29c590e925c3.zip 63323-186 SODIUM CHLORIDE INJECTION [FRESENIUS KABI USA, LLC] 3 Current NDC, Legacy NDC 20241017_f2a98378-9678-4738-9670-fc7a215c0606.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SODIUM CHLORIDE ACTIVE INGREDIENT 451W47IQ8X SODIUM CHLORIDE INJECTION [CARDINAL HEALTH] 1 SODIUM CHLORIDE ACTIVE INGREDIENT 451W47IQ8X SODIUM CHLORIDE INJECTION [APP PHARMACEUTICALS, LLC] 1 SODIUM CHLORIDE ACTIVE INGREDIENT 451W47IQ8X SODIUM CHLORIDE INJECTION [APP PHARMACEUTICALS, LLC] 1 CHLORIDE ION ACTIVE MOIETY Q32ZN48698 SODIUM CHLORIDE INJECTION [CARDINAL HEALTH] 1 CHLORIDE ION ACTIVE MOIETY Q32ZN48698 SODIUM CHLORIDE INJECTION [APP PHARMACEUTICALS, LLC] 1 CHLORIDE ION ACTIVE MOIETY Q32ZN48698 SODIUM CHLORIDE INJECTION [APP PHARMACEUTICALS, LLC] 1 HYDROCHLORIC ACID INACTIVE INGREDIENT QTT17582CB SODIUM CHLORIDE INJECTION [CARDINAL HEALTH] 1 HYDROCHLORIC ACID INACTIVE INGREDIENT QTT17582CB SODIUM CHLORIDE INJECTION [APP PHARMACEUTICALS, LLC] 1 HYDROCHLORIC ACID INACTIVE INGREDIENT QTT17582CB SODIUM CHLORIDE INJECTION [APP PHARMACEUTICALS, LLC] 1 SODIUM HYDROXIDE INACTIVE INGREDIENT 55X04QC32I SODIUM CHLORIDE INJECTION [CARDINAL HEALTH] 1 SODIUM HYDROXIDE INACTIVE INGREDIENT 55X04QC32I SODIUM CHLORIDE INJECTION [APP PHARMACEUTICALS, LLC] 1 SODIUM HYDROXIDE INACTIVE INGREDIENT 55X04QC32I SODIUM CHLORIDE INJECTION [APP PHARMACEUTICALS, LLC] 1
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 2 of 232 · 4,636 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Sweethearts - Be Mine - Sugared Berries ALCOHOL Scent Theory Products LLC 5ac32ffb-926a-f249-e063-6394a90a8d87 2026-09-05 Warnings Exact identifier application number: M003 Sweethearts - UR Sweet - Sweet Cherry Hand Sanitizer ALCOHOL Scent Theory Products LLC 5ac33b21-9192-8baa-e063-6294a90a6e75 2026-09-05 Warnings Exact identifier application number: M003 Sweethearts - Ooo La La - Banana Cream Hand Sanitizer ALCOHOL Scent Theory Products LLC 5ac34dda-fbdf-0ca7-e063-6394a90ab764 2026-09-05 Warnings Exact identifier application number: M003 SurviveX PREP WIPES ALCOHOL PREP PAD Changzhou Maokang Medical Products Co., Ltd. 5a7e9dc6-cf43-7ffc-e063-6394a90a3faa 2026-09-04 Warnings Exact identifier application number: M003 rxcui: 797544 unii: ND2M416302 Members Mark ISOPROPYL ALCOHOL Sams West Inc c251ac50-f74f-4a48-e053-2a95a90aac0d 2026-09-04 Warnings Exact identifier application number: M003 rxcui: 797544 unii: ND2M416302 Walmart ISOPROPYL ALCOHOL Walmart, Inc. 2f1342ef-1843-40a6-e063-6294a90a577f 2026-09-04 Warnings Exact identifier application number: M003 rxcui: 797544 unii: ND2M416302 Curad Alcohol Prep Pads Medium ISOPROPYL ALCOHOL Medline Industries, LP 1ce3872e-2307-4a38-bd7d-7eb2b226cf3c 2026-09-04 Warnings Exact identifier application number: M003 rxcui: 797544 unii: ND2M416302 Alcohol ISOPROPYL ALCOHOL SuperValu, Inc. 5e6e6d6f-4472-40f1-b0a9-96cee7ef075b 2026-09-04 Warnings Exact identifier application number: M003 rxcui: 797544 unii: ND2M416302 Alcohol ISOPROPYL ALCOHOL Foodhold U.S.A. LLC a94c023c-5313-4940-90a7-b3061a8b90e1 2026-09-04 Warnings Exact identifier application number: M003 rxcui: 797544 unii: ND2M416302 Meijer ISOPROPYL ALCOHOL Meijer Distribution Inc ca008d84-cf51-3703-e053-2a95a90a9bf1 2026-09-04 Warnings Exact identifier application number: M003 rxcui: 797544 unii: ND2M416302 Psoriasis Control CENTELLA ASIATICA, SODIUM CHLORIDE, AND SILICON DIOXIDE Forces of Nature 2db33771-0bb9-49f8-84fa-dddc28e4ba26 2026-09-04 Warnings Exact identifier unii: 451W47IQ8X Walmart ISOPROPYL ALCOHOL Walmart, Inc. 2eff98ba-5736-b07e-e063-6394a90aeea9 2026-09-04 Warnings Exact identifier application number: M003 rxcui: 797544 unii: ND2M416302 Walgreen Alcohol ISOPROPYL ALCOHOL Walgreens Company deeae1ea-3d81-4260-95be-c4f328e3fdef 2026-09-04 Warnings Exact identifier application number: M003 rxcui: 797544 unii: ND2M416302 purelax POLYETHYLENE GLYCOL 3350 CVS Pharmacy fc3b6006-a75a-41b3-9f0b-a3152df1363f 2026-09-04 Warnings Exact identifier unii: G2M7P15E5P Dollar General ISOPROPYL ALCOHOL Dollar General Corporation 00b2ef34-42d9-523c-e063-6294a90a753d 2026-09-03 Warnings Exact identifier application number: M003 rxcui: 797544 unii: ND2M416302 Signature Select Alcohol Prep Pads ISOPROPYL ALCOHOL Better Living Brands LLC 31ce72e3-03a3-1608-e063-6394a90ad850 2026-09-03 Warnings Exact identifier application number: M003 rxcui: 797544 unii: ND2M416302 SurviveX Sting Relief STING RELIEF WIPE Changzhou Maokang Medical Products Co., Ltd. 5a83b1f1-c8dc-cf07-e063-6394a90a20ca 2026-09-03 Warnings Exact identifier application number: M003 unii: ND2M416302 SurviveX Antiseptic Wipes BZK ANTISEPTIC CLEANING WIPE Changzhou Maokang Medical Products Co., Ltd. 5a82d9fb-dff8-1c89-e063-6394a90a32c9 2026-09-03 Warnings Exact identifier unii: ND2M416302 basic care clearlax POLYETHYLENE GLYCOL 3350 Amazon.com Services LLC 1ccb8604-34f6-4e1e-beed-eb81d6aa7aef 2026-09-03 Warnings Exact identifier unii: G2M7P15E5P KROGER Saline NASAL KROGER COMPANY c84b242b-f46e-4ea8-a3c1-109a47644646 2026-09-02 Warnings Exact identifier unii: 451W47IQ8X
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.