Magnesium Sulfate inactive ingredients by manufacturer
Wondering whether your Magnesium Sulfate has lactose, gluten, soy, a dye or gelatin in it? The medicine is the same, but the fillers, coatings and colors differ from one company to the next. This page shows what each Magnesium Sulfate product's FDA label lists, so you can find a version that leaves out what you avoid and ask your pharmacist for it by its NDC.
We have read the FDA labels of 44 of the 102 current Magnesium Sulfate products on the market today, from 61 companies listing it with the FDA, and lined them up side by side. 9 labels have no inactive-ingredient list we could read, so those products cannot be compared. 49 labels give only a label-wide paragraph, not a list for the exact product, so they are not compared.
Ask about your bottle
Is there something in your Magnesium Sulfate? Ask in plain words.
Name the company, strength or the NDC on your bottle and the ingredient you avoid. The answer comes only from the FDA labels on this page.
Answers are drawn from the FDA label data on this page and checked against it. They are not medical advice: confirm with your pharmacist before relying on them.
The short answer
Which Magnesium Sulfate products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseNo checked product
No checked Magnesium Sulfate product lists lactose.
-
Wheat or gluten sourceNo checked product
No checked Magnesium Sulfate product lists a wheat or gluten source.
-
SoyNo checked product
No checked Magnesium Sulfate product lists soy.
-
Synthetic dyesNo checked product
No checked Magnesium Sulfate product lists synthetic dyes.
-
GelatinNo checked product
No checked Magnesium Sulfate product lists gelatin.
Also listed by some products: Sugar 4 of 44
Find a version without it
Every current Magnesium Sulfate product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Amazon.com Services LLC 1 product | ||
| 1 g/g topical solutionNDC 72288-0602-04 | Label gives only a general paragraph, not compared | See the product page |
| Amneal Pharmaceuticals LLC 2 products | ||
| 40 mg/mL injectionNDC 70121-1719-02 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 40 mg/mL injectionNDC 70121-1720-03 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Athenex Pharmaceutical Division, LLC. 2 products | ||
| 40 mg/mL injectionNDC 70860-0501-81 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 80 mg/mL injectionNDC 70860-0502-81 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Avenacy, LLC 2 products | ||
| 40 mg/mL injectionNDC 83634-0500-81 | None of these listed |
Show 3 ingredientssodium hydroxide, sulfuric acid, water |
| 80 mg/mL injectionNDC 83634-0501-81 | None of these listed |
Show 3 ingredientssodium hydroxide, sulfuric acid, water |
| B. Braun Medical Inc. 4 products | ||
| 2 g/50 mL injectionNDC 00264-4204-52 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 4 g/50 mL injectionNDC 00264-4205-52 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 4 g/100 mL injectionNDC 00264-4206-54 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 10 mg/mL injectionNDC 00264-4400-54 | Sugar (sucrose, dextrose) |
Show 4 ingredientsDEXTROSE MONOHYDRATE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Baxter Healthcare Corporation 5 products | ||
| 2 g/50 mL injectionNDC 00338-1708-40 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 3 g/100 mL injectionNDC 00338-6353-40 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 4 g/50 mL injectionNDC 00338-1719-40 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 4 g/100 mL injectionNDC 00338-1715-40 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 10 mg/mL injectionNDC 00338-1709-40 | Sugar (sucrose, dextrose) |
Show 4 ingredientsDEXTROSE MONOHYDRATE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Camber Pharmaceuticals, Inc. 1 product | ||
| 500 mg/mL injectionNDC 31722-0394-32 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Cardinal Health (Leader) 70000 1 product | ||
| 1 g/g topical powderNDC 70000-0614-01 | Label gives only a general paragraph, not compared | See the product page |
| Cardinal Health, 110 dba Leader 1 product | ||
| 1 g/g ointment or gel topical creamNDC 70000-0021-01 | Label gives only a general paragraph, not compared | See the product page |
| Chain Drug Consortium, LLC 1 product | ||
| 1 g/g topical powderNDC 68016-0732-01 | Label gives only a general paragraph, not compared | See the product page |
| Chain Drug Marketing Association 1 product | ||
| 1 g/g topical solutionNDC 83324-0175-04 | Label gives only a general paragraph, not compared | See the product page |
| Civica, Inc. 1 product | ||
| 2 g/50 mL injectionNDC 72572-0511-40 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Cvs Pharmacy 1 product | ||
| 1 g/g topical powderNDC 51316-0072-45 | Label gives only a general paragraph, not compared | See the product page |
| CVS Pharmacy, Inc. 1 product | ||
| 1 g/g oral solutionNDC 69842-0602-04 | Label gives only a general paragraph, not compared | See the product page |
| Cvs Pharmacy, Inc 1 product | ||
| 1 g/g topical powderNDC 51316-0395-04 | Label gives only a general paragraph, not compared | See the product page |
| Discount Drug Mart 1 product | ||
| 1 g/g topical solutionNDC 53943-0602-07 | Label gives only a general paragraph, not compared | See the product page |
| Family Dollar (FAMILY WELLNESS) 1 product | ||
| 1 g/g topical powderNDC 55319-0572-02 | Label gives only a general paragraph, not compared | See the product page |
| Filo America 1 product | ||
| 1 kg/kg oral solutionNDC 50438-0001-00 | Label gives only a general paragraph, not compared | See the product page |
| Fresenius Kabi USA, LLC 5 products | ||
| 1 g/100 mL injectionNDC 63323-0108-01 | Sugar (sucrose, dextrose) |
Show 3 ingredientsDEXTROSE MONOHYDRATE, SODIUM HYDROXIDE, SULFURIC ACID |
| 40 mg/mL injectionNDC 63323-0106-01 | None of these listed |
Show 2 ingredientsSODIUM HYDROXIDE, SULFURIC ACID |
| 80 mg/mL injectionNDC 63323-0107-05 | None of these listed |
Show 2 ingredientsSODIUM HYDROXIDE, SULFURIC ACID |
| 500 mg/mL injectionNDC 63323-0064-02 | None of these listed |
Show 2 ingredientsSODIUM HYDROXIDE, SULFURIC ACID |
| 500 mg/mL injectionNDC 63323-0642-20 | No inactive-ingredient list on the label | No list we could read |
| Gland Pharma Limited 2 products | ||
| 2 g/50 mL injectionNDC 68083-0396-01 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 4 g/100 mL injectionNDC 68083-0397-01 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Grocery Outlet, Inc. 1 product | ||
| 1 g/g topical solutionNDC 85828-0602-07 | Label gives only a general paragraph, not compared | See the product page |
| Harris Teeter 1 product | ||
| 1 g/g topical solutionNDC 72036-0602-01 | Label gives only a general paragraph, not compared | See the product page |
| Harris Teeter, LLC 1 product | ||
| 1 g/g topical powderNDC 69256-0395-01 | Label gives only a general paragraph, not compared | See the product page |
| Henry Schein, Inc. 3 products | ||
| 500 mg/mL injectionNDC 00404-9902-20 | No inactive-ingredient list on the label | No list we could read |
| 500 mg/mL injectionNDC 00404-9903-10 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 500 mg/mL injectionNDC 00404-9904-02 | None of these listed |
Show 2 ingredientsSODIUM HYDROXIDE, SULFURIC ACID |
| HF Acquisition Co LLC, DBA HealthFirst 4 products | ||
| 40 mg/mL injectionNDC 51662-1352-01 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 40 mg/mL injectionNDC 51662-1373-01 | None of these listed |
Show 2 ingredientsSODIUM HYDROXIDE, SULFURIC ACID |
| 500 mg/mL injectionNDC 51662-1372-01 | No inactive-ingredient list on the label | No list we could read |
| 500 mg/mL injectionNDC 51662-1390-01 | None of these listed |
Show 2 ingredientsSODIUM HYDROXIDE, SULFURIC ACID |
| Hospira, Inc. 8 products | ||
| 2 g/50 mL injectionNDC 00409-5239-24 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 4 g/100 mL injectionNDC 00409-4121-24 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 10 mg/mL injectionNDC 00409-6727-23 | Sugar (sucrose, dextrose) |
Show 4 ingredientsDEXTROSE MONOHYDRATE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 20 g/500 mL injectionNDC 00409-2050-20 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 40 g/1000 mL injectionNDC 00409-3164-12 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 40 mg/mL injectionNDC 00409-6729-03 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 500 mg/mL injectionNDC 00409-1754-10 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 500 mg/mL injectionNDC 00409-2168-77 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Humco Holding Group, Inc. 1 product | ||
| 1000 mg/g oral solutionNDC 00395-0807-16 | None of these listed |
Show 1 ingredientWATER |
| Hy-Vee, Inc. 1 product | ||
| 1 g/g topical solutionNDC 42507-0962-06 | Label gives only a general paragraph, not compared | See the product page |
| International Wholesale Inc. 2 products | ||
| 100 g/100 g topical powderNDC 52862-0202-01 | Label gives only a general paragraph, not compared | See the product page |
| 100 g/100 g topical powderNDC 52862-0203-01 | Label gives only a general paragraph, not compared | See the product page |
| J C Sales 2 products | ||
| 100 g/100 g oral powderNDC 72520-0001-12 | Label gives only a general paragraph, not compared | See the product page |
| 100 g/100 g oral powderNDC 72520-0002-12 | Label gives only a general paragraph, not compared | See the product page |
| Jell Pharmaceuticals Pvt. Ltd. 1 product | ||
| 100 g/100 g oral powderNDC 30400-0210-01 | Label gives only a general paragraph, not compared | See the product page |
| Medical Purchasing Solutions, LLC 3 products | ||
| 500 mg/mL injectionNDC 71872-7142-01 | None of these listed |
Show 2 ingredientsSODIUM HYDROXIDE, SULFURIC ACID |
| 500 mg/mL injectionNDC 71872-7229-01 | None of these listed |
Show 2 ingredientsSODIUM HYDROXIDE, SULFURIC ACID |
| 500 mg/mL injectionNDC 71872-7381-01 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Meijer, Inc. 2 products | ||
| 1 g/g oral powderNDC 41250-0929-07 | Label gives only a general paragraph, not compared | See the product page |
| 1 g/g topical solutionNDC 41250-0602-07 | Label gives only a general paragraph, not compared | See the product page |
| Menper Distributors, Inc 1 product | ||
| 1 g/g other oral formNDC 53145-0580-01 | Label gives only a general paragraph, not compared | See the product page |
| New Pride Corp 1 product | ||
| 100 g/100 g oral powderNDC 58037-0008-01 | Label gives only a general paragraph, not compared | See the product page |
| Old East Main Co. 1 product | ||
| 1 g/g topical solutionNDC 55910-0038-07 | Label gives only a general paragraph, not compared | See the product page |
| Pharmadel LLC 1 product | ||
| 1 g/g other oral formNDC 55758-0419-03 | Label gives only a general paragraph, not compared | See the product page |
| ProPharma Distribution 1 product | ||
| 500 mg/mL injectionNDC 84549-0064-03 | None of these listed |
Show 2 ingredientsSODIUM HYDROXIDE, SULFURIC ACID |
| Publix Super Markets, Inc. 1 product | ||
| 1 g/g oral powderNDC 56062-0952-07 | Label gives only a general paragraph, not compared | See the product page |
| Remedyrepack Inc. 1 product | ||
| 500 mg/mL injectionNDC 70518-4375-00 | None of these listed |
Show 2 ingredientsSODIUM HYDROXIDE, SULFURIC ACID |
| Retail Business Services, LLC 1 product | ||
| 1 g/g topical solutionNDC 72476-0602-04 | Label gives only a general paragraph, not compared | See the product page |
| Safeway, Inc. 1 product | ||
| 1 g/g topical powderNDC 21130-0970-04 | Label gives only a general paragraph, not compared | See the product page |
| Safeway Inc 1 product | ||
| 1 g/g topical solutionNDC 21130-0602-01 | Label gives only a general paragraph, not compared | See the product page |
| Sagent Pharmaceuticals 1 product | ||
| 40 mg/mL injectionNDC 25021-0612-81 | None of these listed |
Show 4 ingredientsNitrogen, Sodium Hydroxide, Sulfuric Acid, Water |
| Sam's West, Inc 1 product | ||
| 1 g/g topical powderNDC 68196-0395-07 | Label gives only a general paragraph, not compared | See the product page |
| Strategic Sourcing Services LLC 1 product | ||
| 1 g/g topical powderNDC 62011-0362-01 | Label gives only a general paragraph, not compared | See the product page |
| Sun Pharmaceutical Industries, Inc. 1 product | ||
| 40 mg/mL injectionNDC 47335-0992-01 | None of these listed |
Show 3 ingredientsSODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Target Corporation 3 products | ||
| 1 g/g topical powderNDC 82442-0017-45 | Label gives only a general paragraph, not compared | See the product page |
| 1 g/g topical solutionNDC 11673-0200-45 | Label gives only a general paragraph, not compared | See the product page |
| 1 g/g topical solutionNDC 11673-0602-01 | Label gives only a general paragraph, not compared | See the product page |
| TOP CARE (Topco Associates LLC) 1 product | ||
| 1 g/g topical powderNDC 36800-0395-01 | Label gives only a general paragraph, not compared | See the product page |
| Topco Associates LLC 2 products | ||
| 1 g/g topical solutionNDC 36800-0602-07 | Label gives only a general paragraph, not compared | See the product page |
| 1 g/g topical solutionNDC 76162-0029-80 | Label gives only a general paragraph, not compared | See the product page |
| United Natural Foods, Inc. dba UNFI 1 product | ||
| 1 g/g topical solutionNDC 41163-0602-07 | Label gives only a general paragraph, not compared | See the product page |
| Universal Distribution Center LLC 1 product | ||
| 100 g/100 g oral powderNDC 52000-0420-16 | Label gives only a general paragraph, not compared | See the product page |
| Valu Merchandisers Company 1 product | ||
| 1 g/g topical solutionNDC 63941-0602-07 | Label gives only a general paragraph, not compared | See the product page |
| Vi-Jon, LLC 1 product | ||
| 1 g/g topical solutionNDC 00869-0602-07 | Label gives only a general paragraph, not compared | See the product page |
| Walgreen Co. 1 product | ||
| 1 g/g topical solutionNDC 00363-0942-05 | Label gives only a general paragraph, not compared | See the product page |
| Walgreens 1 product | ||
| 1 g/g topical powderNDC 00363-0395-01 | Label gives only a general paragraph, not compared | See the product page |
| WG Critical Care, LLC 6 products | ||
| 1 g/100 mL injectionNDC 44567-0410-24 | No inactive-ingredient list on the label | No list we could read |
| 2 g/50 mL injectionNDC 44567-0420-24 | No inactive-ingredient list on the label | No list we could read |
| 4 g/50 mL injectionNDC 44567-0424-24 | No inactive-ingredient list on the label | No list we could read |
| 4 g/100 mL injectionNDC 44567-0421-24 | No inactive-ingredient list on the label | No list we could read |
| 20 g/500 mL injectionNDC 44567-0422-24 | No inactive-ingredient list on the label | No list we could read |
| 40 g/1000 mL injectionNDC 44567-0423-10 | No inactive-ingredient list on the label | No list we could read |
| Whole Foods Market 2 products | ||
| 1 g/g topical powderNDC 42681-6412-01 | Label gives only a general paragraph, not compared | See the product page |
| 1 g/g topical powderNDC 42681-6413-01 | Label gives only a general paragraph, not compared | See the product page |
| Whole Foods Market, Inc. 1 product | ||
| 1 g/g topical solutionNDC 42681-0060-01 | Label gives only a general paragraph, not compared | See the product page |
| WinCo Foods, LLC 1 product | ||
| 1 g/g topical powderNDC 67091-0352-04 | Label gives only a general paragraph, not compared | See the product page |
| Your Military Exchanges 1 product | ||
| 1 g/g topical solutionNDC 55301-0602-07 | Label gives only a general paragraph, not compared | See the product page |
A product with none of these listed is not certified to be without them: the label says what the manufacturer declared, and the source of a starch or a flavor is often not stated. The companies are the FDA's labelers, which include repackagers and distributors selling another company's product under their own label. The NDC opens the product's own page, with the full label and its inactive-ingredient notes.
Magnesium Sulfate without sugar (sucrose or dextrose)
Sugar (sucrose, dextrose): A consideration in diabetes, mostly in liquids and chewables. 4 of 44 checked products list sugar (sucrose or dextrose); 40 do not.
Does not list sugar (sucrose or dextrose)
- Amneal: 40 mg/mL injection (NDC 70121-1719-02), 40 mg/mL injection (NDC 70121-1720-03)
- Athenex Pharmaceutical Division: 40 mg/mL injection, 80 mg/mL injection
- Avenacy: 40 mg/mL injection, 80 mg/mL injection
- B. Braun Medical: 2 g/50 mL injection, 4 g/50 mL injection, 4 g/100 mL injection
- Baxter Healthcare: 2 g/50 mL injection, 3 g/100 mL injection, 4 g/50 mL injection, 4 g/100 mL injection
- Camber: 500 mg/mL injection
- Civica: 2 g/50 mL injection
- Fresenius Kabi: 40 mg/mL injection, 80 mg/mL injection, 500 mg/mL injection
- Gland: 2 g/50 mL injection, 4 g/100 mL injection
- Henry Schein: 500 mg/mL injection (NDC 00404-9903-10), 500 mg/mL injection (NDC 00404-9904-02)
- HF Acquisition Co LLC, DBA HealthFirst: 40 mg/mL injection (NDC 51662-1352-01), 40 mg/mL injection (NDC 51662-1373-01), 500 mg/mL injection
- Hospira: 2 g/50 mL injection, 4 g/100 mL injection, 20 g/500 mL injection, 40 g/1000 mL injection, 40 mg/mL injection, 500 mg/mL injection (NDC 00409-1754-10), 500 mg/mL injection (NDC 00409-2168-77)
- Humco: 1000 mg/g oral solution
- Medical Purchasing Solutions: 500 mg/mL injection (NDC 71872-7142-01), 500 mg/mL injection (NDC 71872-7229-01), 500 mg/mL injection (NDC 71872-7381-01)
- ProPharma Distribution: 500 mg/mL injection
- Remedyrepack: 500 mg/mL injection
- Sagent: 40 mg/mL injection
- Sun: 40 mg/mL injection
Lists sugar (sucrose or dextrose)
- B. Braun Medical: 10 mg/mL injection
- Baxter Healthcare: 10 mg/mL injection
- Fresenius Kabi: 1 g/100 mL injection
- Hospira: 10 mg/mL injection
At the pharmacy counter
How to use this at the pharmacy counter
- Pick the company whose list suits you and copy the NDC from the table. Many pharmacies order from wholesalers that carry several companies' versions and can request a particular one if you ask before the prescription is filled; some buy from one contracted source only, and a few insurance plans cover only certain NDCs, so ask the pharmacist to check.
- Treat "does not list" as exactly that. The label is what the manufacturer declared; a flavor or a starch may have an unstated source, and lines change. For celiac disease or a serious allergy, ask the manufacturer's medical information line for a written statement about the lot you have.
- Check the bottle each refill. A different company usually means a different shape, color and inactive-ingredient list; the pharmacist can tell you who made it, and the two-NDC comparison shows the difference line by line.
- If you need one company's version kept constant, ask your prescriber to write that company or the NDC on the prescription and tell the pharmacy you need it held. Rules vary by state and plan, so confirm with the pharmacist.
Common questions about Magnesium Sulfate inactive ingredients
Is Magnesium Sulfate gluten-free?
Does Magnesium Sulfate contain lactose?
Does Magnesium Sulfate contain soy?
Is there a dye-free Magnesium Sulfate?
Does Magnesium Sulfate contain gelatin?
Why do the inactive ingredients differ between manufacturers?
Can my pharmacy give me a specific manufacturer's version?
How current is this list?
Sources: the products are the finished Magnesium Sulfate products in the FDA's current NDC directory (openFDA), as of October 6, 2026; each inactive-ingredient list is the manufacturer's FDA Structured Product Label via DailyMed, as our label sync last read it. The concern groups are HelloPharmacist's classification of the names the label declares. Educational information only, not medical advice; confirm with your pharmacist before relying on a list. ← Back to the Magnesium Sulfate guide