Inactive ingredients by manufacturer

Sevelamer inactive ingredients by manufacturer

Wondering whether your Sevelamer 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 Sevelamer 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 54 of the 66 current Sevelamer products on the market today, from 37 companies listing it with the FDA, and lined them up side by side. 12 are still being read and will appear on a later visit.

Ask about your bottle

Is there something in your Sevelamer? 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 Sevelamer products list lactose, a gluten source, soy, dyes or gelatin?

  1. LactoseDiffers by manufacturer
  2. Wheat or gluten sourceNo checked product

    No checked Sevelamer product lists a wheat or gluten source.

  3. SoyDiffers by manufacturer
  4. Synthetic dyesNo checked product

    No checked Sevelamer product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Sevelamer product lists gelatin.

Also listed by some products: Corn 3 of 54 Titanium dioxide 6 of 54 Carmine or shellac 24 of 54 Propylene glycol 36 of 54 PEG or polysorbate 7 of 54 Sorbitol or mannitol 18 of 54

Find a version without it

Every current Sevelamer product and what its label lists

Hide products that list:

ProductListsInactive ingredients on the label
AiPing Pharmaceutical, Inc. 1 product
800 mg tabletNDC 11788-0116-07 Still being read Not read yet
American Health Packaging 2 products
800 mg tabletNDC 60687-0328-31 Still being read Not read yet
800 mg tabletNDC 60687-0449-01 Still being read Not read yet
Amneal Pharmaceuticals LLC 1 product
800 mg tabletNDC 65162-0058-03 Carmine or shellac Propylene glycol
Show 9 ingredients

AMMONIA, CELLULOSE, MICROCRYSTALLINE, DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, HYPROMELLOSES, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, ZINC STEARATE

Amneal Pharmaceuticals of New York LLC 2 products
800 mg oral suspensionNDC 00115-1365-29 Propylene glycol
Show 6 ingredients

LEMON, MICROCRYSTALLINE CELLULOSE 102, PROPYLENE GLYCOL ALGINATE, SILICON DIOXIDE, SODIUM CHLORIDE, SUCRALOSE

2400 mg oral suspensionNDC 00115-1366-29 Propylene glycol
Show 6 ingredients

LEMON, MICROCRYSTALLINE CELLULOSE 102, PROPYLENE GLYCOL ALGINATE, SILICON DIOXIDE, SODIUM CHLORIDE, SUCRALOSE

Atlantic Biologicals Corp. 1 product
800 mg tabletNDC 17856-0921-01 Carmine or shellac Propylene glycol Sorbitol or mannitol
Show 12 ingredients

AMMONIA, CROSPOVIDONE (120 .MU.M), DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, GLYCERYL DIBEHENATE, HYDROXYPROPYL CELLULOSE (90000 WAMW), HYPROMELLOSE, UNSPECIFIED, MANNITOL, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, TALC

Aurobindo Pharma Limited 5 products
800 mg oral suspensionNDC 65862-0930-90 None of these listed
Show 4 ingredients

FERRIC OXIDE YELLOW, ORANGE, SUCRALOSE, XANTHAN GUM

2400 mg oral suspensionNDC 65862-0931-90 Still being read Not read yet
400 mg tabletNDC 59651-0087-36 Carmine or shellac Propylene glycol
Show 12 ingredients

AMMONIA, CROSPOVIDONE (120 .MU.M), DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, GLYCERYL DIBEHENATE, HYDROXYPROPYL CELLULOSE (90000 WAMW), HYPROMELLOSE, UNSPECIFIED, MICROCRYSTALLINE CELLULOSE, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, TALC

800 mg tabletNDC 59651-0088-18 Carmine or shellac Propylene glycol
Show 12 ingredients

AMMONIA, CROSPOVIDONE (120 .MU.M), DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, GLYCERYL DIBEHENATE, HYDROXYPROPYL CELLULOSE (90000 WAMW), HYPROMELLOSE, UNSPECIFIED, MICROCRYSTALLINE CELLULOSE, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, TALC

800 mg tabletNDC 65862-0921-18 Carmine or shellac Propylene glycol Sorbitol or mannitol
Show 12 ingredients

AMMONIA, CROSPOVIDONE (120 .MU.M), DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, GLYCERYL DIBEHENATE, HYDROXYPROPYL CELLULOSE (90000 WAMW), HYPROMELLOSE, UNSPECIFIED, MANNITOL, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, TALC

AvKARE 1 product
800 mg tabletNDC 73190-0014-27 Titanium dioxide Propylene glycol Polyethylene glycol or polysorbate
Show 10 ingredients

CARNAUBA WAX, FERROSOFERRIC OXIDE, HYDROXYPROPYL CELLULOSE, UNSPECIFIED, HYPROMELLOSE, UNSPECIFIED, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, PROPYLENE GLYCOL, SODIUM CHLORIDE, TITANIUM DIOXIDE, ZINC STEARATE

AvPAK 1 product
800 mg tabletNDC 50268-0720-15 Carmine or shellac Propylene glycol
Show 9 ingredients

AMMONIA, CELLULOSE, MICROCRYSTALLINE, DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, HYPROMELLOSES, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, ZINC STEARATE

Bionpharma Inc. 2 products
800 mg oral suspensionNDC 69452-0126-19 Propylene glycol
Show 4 ingredients

PROPYLENE GLYCOL ALGINATE, SILICON DIOXIDE, SODIUM CHLORIDE, SUCRALOSE

2400 mg oral suspensionNDC 69452-0127-19 Propylene glycol
Show 4 ingredients

PROPYLENE GLYCOL ALGINATE, SILICON DIOXIDE, SODIUM CHLORIDE, SUCRALOSE

Bryant Ranch Prepack 3 products
400 mg tabletNDC 72162-2500-02 Carmine or shellac Propylene glycol
Show 9 ingredients

AMMONIA, DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MICROCRYSTALLINE CELLULOSE, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, STEARIC ACID

800 mg tabletNDC 72162-2499-01 Carmine or shellac Propylene glycol
Show 10 ingredients

AMMONIA, DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, HYDROXYPROPYL CELLULOSE (1600000 WAMW), HYPROMELLOSE, UNSPECIFIED, MICROCRYSTALLINE CELLULOSE, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, ZINC STEARATE

800 mg tabletNDC 72162-2501-02 Carmine or shellac Propylene glycol
Show 9 ingredients

AMMONIA, DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MICROCRYSTALLINE CELLULOSE, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, STEARIC ACID

Cardinal Health 107, LLC 3 products
800 mg injectionNDC 55154-2647-00 Still being read Not read yet
800 mg tabletNDC 55154-3358-00 Soy Carmine or shellac Propylene glycol Sorbitol or mannitol
Show 13 ingredients

AMMONIA, CROSPOVIDONE (120 .MU.M), FERROSOFERRIC OXIDE, HYDROXYPROPYL CELLULOSE (110000 WAMW), MANNITOL, POLYVINYL ALCOHOL, UNSPECIFIED, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, SOYBEAN LECITHIN, TALC, XANTHAN GUM, ZINC STEARATE

800 mg tabletNDC 55154-8188-00 Still being read Not read yet
Cipla USA Inc. 2 products
800 mg tabletNDC 69097-0893-93 None of these listed
Show 8 ingredients

CROSPOVIDONE, UNSPECIFIED, DIACETYLATED MONOGLYCERIDES, HYDROXYPROPYL CELLULOSE, UNSPECIFIED, HYPROMELLOSE, UNSPECIFIED, MICROCRYSTALLINE CELLULOSE, SILICON DIOXIDE, SODIUM STEARYL FUMARATE, TALC

800 mg tabletNDC 69097-0967-93 None of these listed
Show 8 ingredients

CROSPOVIDONE, UNSPECIFIED, DIACETYLATED MONOGLYCERIDES, HYDROXYPROPYL CELLULOSE, UNSPECIFIED, HYPROMELLOSE, UNSPECIFIED, MICROCRYSTALLINE CELLULOSE, SILICON DIOXIDE, SODIUM STEARYL FUMARATE, TALC

Dr. Reddy's Laboratories Limited 1 product
800 mg tabletNDC 55111-0789-11 Soy Carmine or shellac Propylene glycol Sorbitol or mannitol
Show 13 ingredients

Ammonia, Crospovidone, Ferrosoferric Oxide, HYDROXYPROPYL CELLULOSE (110000 WAMW), Lecithin, Soybean, Mannitol, Polyvinyl Alcohol, Propylene Glycol, Shellac, Silicon Dioxide, Talc, Xanthan Gum, Zinc Stearate

Dr. Reddys Laboratories Inc 2 products
800 mg oral suspensionNDC 43598-0478-90 Still being read Not read yet
2400 mg oral suspensionNDC 43598-0479-90 Propylene glycol Sorbitol or mannitol
Show 8 ingredients

Ferric Oxide Yellow, Lemon, Mannitol, Orange, Propylene Glycol, Silicon Dioxide, Sucralose, Vanilla

Exelan Pharmaceuticals Inc. 2 products
800 mg tabletNDC 76282-0407-27 None of these listed
Show 8 ingredients

CELLULOSE, MICROCRYSTALLINE, CROSPOVIDONE, UNSPECIFIED, DIACETYLATED MONOGLYCERIDES, HYDROXYPROPYL CELLULOSE, UNSPECIFIED, HYPROMELLOSE, UNSPECIFIED, SILICON DIOXIDE, SODIUM STEARYL FUMARATE, TALC

800 mg tabletNDC 76282-0664-27 None of these listed
Show 8 ingredients

CROSPOVIDONE, UNSPECIFIED, DIACETYLATED MONOGLYCERIDES, HYDROXYPROPYL CELLULOSE, UNSPECIFIED, HYPROMELLOSE, UNSPECIFIED, MICROCRYSTALLINE CELLULOSE, SILICON DIOXIDE, SODIUM STEARYL FUMARATE, TALC

Genzyme Corporation 3 products
800 mg oral suspensionNDC 58468-0132-02 Propylene glycol
Show 4 ingredients

FERRIC OXIDE YELLOW, PROPYLENE GLYCOL ALGINATE, SODIUM CHLORIDE, SUCRALOSE

2400 mg oral suspensionNDC 58468-0131-02 Propylene glycol
Show 4 ingredients

FERRIC OXIDE YELLOW, PROPYLENE GLYCOL ALGINATE, SODIUM CHLORIDE, SUCRALOSE

800 mg tabletNDC 58468-0133-01 Still being read Not read yet
Glenmark Pharmaceuticals Inc., USA 2 products
800 mg injectionNDC 68462-0447-18 Lactose Corn-derived Carmine or shellac Propylene glycol Sorbitol or mannitol
Show 15 ingredients

AMMONIA, BUTYL ALCOHOL, DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, HYPROMELLOSE 2910 (50 MPA.S), HYPROMELLOSE, UNSPECIFIED, ISOPROPYL ALCOHOL, LACTOSE MONOHYDRATE, MANNITOL, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, STARCH, CORN, TALC, ZINC STEARATE

400 mg tabletNDC 68462-0446-26 Lactose Corn-derived Carmine or shellac Propylene glycol Sorbitol or mannitol
Show 15 ingredients

AMMONIA, BUTYL ALCOHOL, DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, HYPROMELLOSE 2910 (50 MPA.S), HYPROMELLOSE, UNSPECIFIED, ISOPROPYL ALCOHOL, LACTOSE MONOHYDRATE, MANNITOL, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, STARCH, CORN, TALC, ZINC STEARATE

Golden State Medical Supply, Inc. 1 product
800 mg tabletNDC 51407-0706-27 Soy Carmine or shellac Propylene glycol Sorbitol or mannitol
Show 13 ingredients

AMMONIA, CROSPOVIDONE, FERROSOFERRIC OXIDE, HYDROXYPROPYL CELLULOSE (110000 WAMW), LECITHIN, SOYBEAN, MANNITOL, POLYVINYL ALCOHOL, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, TALC, XANTHAN GUM, ZINC STEARATE

Insignamedex Llc 1 product
800 mg tabletNDC 87367-0266-12 None of these listed
Show 5 ingredients

DIACETYLATED MONOGLYCERIDES, HYPROMELLOSE, UNSPECIFIED, MICROCRYSTALLINE CELLULOSE, SILICON DIOXIDE, ZINC STEARATE

Lupin Pharmaceuticals, Inc. 1 product
800 mg tabletNDC 70748-0173-26 Carmine or shellac Propylene glycol Polyethylene glycol or polysorbate
Show 9 ingredients

FERROSOFERRIC OXIDE, POLYETHYLENE GLYCOL 3350, POLYETHYLENE GLYCOL 6000, POLYVINYL ALCOHOL, UNSPECIFIED, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, STEARIC ACID, TALC

Macleods Pharmaceuticals Limited 5 products
0.8 g oral suspensionNDC 33342-0288-68 Sorbitol or mannitol
Show 6 ingredients

FERRIC OXIDE YELLOW, MANNITOL, POVIDONE K30, SODIUM CHLORIDE, SUCRALOSE, XANTHAN GUM

2.4 g oral suspensionNDC 33342-0289-68 Sorbitol or mannitol
Show 6 ingredients

FERRIC OXIDE YELLOW, MANNITOL, POVIDONE K30, SODIUM CHLORIDE, SUCRALOSE, XANTHAN GUM

400 mg tabletNDC 33342-0241-65 Carmine or shellac Propylene glycol
Show 9 ingredients

AMMONIA, CELLULOSE, MICROCRYSTALLINE, DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, HYPROMELLOSES, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, STEARIC ACID

800 mg tabletNDC 33342-0215-56 Carmine or shellac Propylene glycol
Show 10 ingredients

AMMONIA, CELLULOSE, MICROCRYSTALLINE, DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, HYDROXYPROPYL CELLULOSE, HYPROMELLOSES, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, ZINC STEARATE

800 mg tabletNDC 33342-0242-07 Carmine or shellac Propylene glycol
Show 9 ingredients

AMMONIA, CELLULOSE, MICROCRYSTALLINE, DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, HYPROMELLOSES, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, STEARIC ACID

Major Pharmaceuticals 2 products
800 mg injectionNDC 00904-7209-06 Lactose Corn-derived Carmine or shellac Propylene glycol Sorbitol or mannitol
Show 15 ingredients

AMMONIA, BUTYL ALCOHOL, DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, HYPROMELLOSE 2910 (50 MPA.S), HYPROMELLOSE, UNSPECIFIED, ISOPROPYL ALCOHOL, LACTOSE MONOHYDRATE, MANNITOL, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, STARCH, CORN, TALC, ZINC STEARATE

800 mg tabletNDC 00904-6707-06 Still being read Not read yet
Marp Pharma 1 product
800 mg tabletNDC 85898-0101-27 None of these listed
Show 5 ingredients

DIACETYLATED MONOGLYCERIDES, HYPROMELLOSE, UNSPECIFIED, MICROCRYSTALLINE CELLULOSE, SILICON DIOXIDE, ZINC STEARATE

Navinta LLC 1 product
800 mg tabletNDC 68475-0010-01 Titanium dioxide Polyethylene glycol or polysorbate
Show 11 ingredients

COPOVIDONE K25-31, HYDROXYPROPYL CELLULOSE (1600000 WAMW), HYDROXYPROPYL CELLULOSE (90000 WAMW), HYPROMELLOSE 2910 (15 MPA.S), HYPROMELLOSE 2910 (6 MPA.S), MICROCRYSTALLINE CELLULOSE 105, POLYETHYLENE GLYCOL 6000, SILICON DIOXIDE, SODIUM STEARYL FUMARATE, TITANIUM DIOXIDE, WATER

NCS HealthCare of KY, LLC dba Vangard Labs 1 product
800 mg tabletNDC 00615-8239-05 Carmine or shellac Propylene glycol Sorbitol or mannitol
Show 12 ingredients

AMMONIA, CROSPOVIDONE (120 .MU.M), DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, GLYCERYL DIBEHENATE, HYDROXYPROPYL CELLULOSE (90000 WAMW), HYPROMELLOSE, UNSPECIFIED, MANNITOL, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, TALC

NorthStar Rx LLC 1 product
800 mg tabletNDC 16714-0814-01 Carmine or shellac Propylene glycol Sorbitol or mannitol
Show 12 ingredients

AMMONIA, CROSPOVIDONE (120 .MU.M), DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, GLYCERYL DIBEHENATE, HYDROXYPROPYL CELLULOSE (90000 WAMW), HYPROMELLOSE, UNSPECIFIED, MANNITOL, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, TALC

NorthStar RxLLC 1 product
0.8 g oral suspensionNDC 72603-0398-02 Sorbitol or mannitol
Show 6 ingredients

FERRIC OXIDE YELLOW, MANNITOL, POVIDONE K30, SODIUM CHLORIDE, SUCRALOSE, XANTHAN GUM

PD-Rx Pharmaceuticals, Inc. 1 product
800 mg tabletNDC 72789-0562-94 Sorbitol or mannitol
Show 9 ingredients

CROSPOVIDONE, DIACETYLATED MONOGLYCERIDES, GLYCERYL DIBEHENATE, HYDROXYPROPYL CELLULOSE, UNSPECIFIED, HYPROMELLOSE 2910 (3 MPA.S), HYPROMELLOSE 2910 (6 MPA.S), MANNITOL, SILICON DIOXIDE, TALC

Precision Dose, Inc. 1 product
800 mg tabletNDC 68094-0034-64 Carmine or shellac Propylene glycol
Show 9 ingredients

Ammonia, DIACETYLATED MONOGLYCERIDES, Ferrosoferric Oxide, Hypromellose, Unspecified, Microcrystalline Cellulose, Propylene Glycol, Shellac, Silicon Dioxide, Zinc Stearate

Proficient Rx LP 1 product
800 mg tabletNDC 71205-0966-67 Titanium dioxide Propylene glycol Polyethylene glycol or polysorbate
Show 10 ingredients

CARNAUBA WAX, FERROSOFERRIC OXIDE, HYDROXYPROPYL CELLULOSE, UNSPECIFIED, HYPROMELLOSE, UNSPECIFIED, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, PROPYLENE GLYCOL, SODIUM CHLORIDE, TITANIUM DIOXIDE, ZINC STEARATE

Sanofi-Aventis U.S. LLC 4 products
0.8 g oral suspensionNDC 00955-1052-90 Propylene glycol
Show 4 ingredients

FERRIC OXIDE YELLOW, PROPYLENE GLYCOL ALGINATE, SODIUM CHLORIDE, SUCRALOSE

2.4 g oral suspensionNDC 00955-1054-90 Propylene glycol
Show 4 ingredients

FERRIC OXIDE YELLOW, PROPYLENE GLYCOL ALGINATE, SODIUM CHLORIDE, SUCRALOSE

800 mg tabletNDC 00955-1050-27 None of these listed
Show 6 ingredients

DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MICROCRYSTALLINE CELLULOSE, SODIUM CHLORIDE, ZINC STEARATE

800 mg tabletNDC 00955-1057-30 Still being read Not read yet
Shandong Xinhua Pharmaceutical Co., Ltd. 1 product
800 mg tabletNDC 58624-5001-02 Sorbitol or mannitol
Show 9 ingredients

CROSPOVIDONE, DIACETYLATED MONOGLYCERIDES, GLYCERYL BEHENATE/EICOSADIOATE, HYDROXYPROPYL CELLULOSE, UNSPECIFIED, HYPROMELLOSE 2910 (3 MPA.S), HYPROMELLOSE 2910 (6 MPA.S), MANNITOL, SILICON DIOXIDE, TALC

Strides Pharma Science Limited 3 products
800 mg/930 mg oral suspensionNDC 64380-0880-80 Sorbitol or mannitol
Show 4 ingredients

FERRIC OXIDE YELLOW, MANNITOL, NEOTAME, SODIUM CHLORIDE

2400 mg/2790 mg oral suspensionNDC 64380-0881-80 Sorbitol or mannitol
Show 4 ingredients

FERRIC OXIDE YELLOW, MANNITOL, NEOTAME, SODIUM CHLORIDE

800 mg tabletNDC 64380-0872-04 Carmine or shellac
Show 11 ingredients

CROSPOVIDONE, DIACETYLATED MONOGLYCERIDES, FERROSOFERRIC OXIDE, HYPROMELLOSE 2910 (15 MPA.S), HYPROMELLOSE 2910 (5 MPA.S), MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POVIDONE, SHELLAC, SILICON DIOXIDE, SODIUM CHLORIDE

TWi Pharmaceuticals, Inc. 1 product
800 mg tabletNDC 24979-0186-46 Titanium dioxide Propylene glycol Polyethylene glycol or polysorbate
Show 10 ingredients

CARNAUBA WAX, FERROSOFERRIC OXIDE, HYDROXYPROPYL CELLULOSE, UNSPECIFIED, HYPROMELLOSE, UNSPECIFIED, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, PROPYLENE GLYCOL, SODIUM CHLORIDE, TITANIUM DIOXIDE, ZINC STEARATE

Westminster Pharmaceuticals, LLC 1 product
800 mg tabletNDC 69367-0423-27 Titanium dioxide Propylene glycol Polyethylene glycol or polysorbate
Show 10 ingredients

CARNAUBA WAX, FERROSOFERRIC OXIDE, HYDROXYPROPYL CELLULOSE, UNSPECIFIED, HYPROMELLOSE, UNSPECIFIED, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, PROPYLENE GLYCOL, SODIUM CHLORIDE, TITANIUM DIOXIDE, ZINC STEARATE

Zydus Pharmaceuticals USA Inc. 3 products
800 mg tabletNDC 68382-0824-10 Still being read Not read yet
800 mg tabletNDC 70710-2058-08 Still being read Not read yet
800 mg tabletNDC 70710-2170-03 Titanium dioxide Polyethylene glycol or polysorbate
Show 11 ingredients

COPOVIDONE K25-31, HYDROXYPROPYL CELLULOSE (1600000 WAMW), HYDROXYPROPYL CELLULOSE (90000 WAMW), HYPROMELLOSE 2910 (15 MPA.S), HYPROMELLOSE 2910 (6 MPA.S), MICROCRYSTALLINE CELLULOSE 105, POLYETHYLENE GLYCOL 6000, SILICON DIOXIDE, SODIUM STEARYL FUMARATE, TITANIUM DIOXIDE, WATER

Zydus Lifesciences Limited 1 product
800 mg tabletNDC 70771-1520-00 Lactose Carmine or shellac Propylene glycol
Show 18 ingredients

CASTOR OIL, CROSPOVIDONE (15 MPA.S AT 5%), DIBUTYL SEBACATE, FERROSOFERRIC OXIDE, HYPROMELLOSE 2910 (15 MPA.S), HYPROMELLOSE 2910 (5 MPA.S), HYPROMELLOSE 2910 (50 MPA.S), HYPROMELLOSE 2910 (6 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYVINYL ALCOHOL, UNSPECIFIED, POVIDONE K90, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, TRIACETIN, WATER

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.

Sevelamer without lactose

Lactose: milk sugar; a concern with lactose intolerance or a milk allergy. 4 of 54 checked products list lactose; 50 do not.

Does not list lactose

Lists lactose

Sevelamer without soy

Soy: soybean oil or soy lecithin; a concern with soy allergy. 3 of 54 checked products list soy; 51 do not.

Does not list soy

Lists soy

Sevelamer without corn-derived ingredients

Corn-derived: corn starch, maize or corn syrup; a concern with corn allergy. 3 of 54 checked products list corn-derived ingredients; 51 do not.

Does not list corn-derived ingredients

Lists corn-derived ingredients

Sevelamer without titanium dioxide

Titanium dioxide: A white colorant some people choose to avoid. 6 of 54 checked products list titanium dioxide; 48 do not.

Does not list titanium dioxide

Lists titanium dioxide

Sevelamer without carmine or shellac

Carmine or shellac: insect-derived red colorant or coating glaze. 24 of 54 checked products list carmine or shellac; 30 do not.

Lists carmine or shellac

Sevelamer without propylene glycol

Propylene glycol: A solvent in liquids and capsules; a concern in kidney disease, for infants, and at high doses. 36 of 54 checked products list propylene glycol; 18 do not.

Lists propylene glycol

Sevelamer without polyethylene glycol or polysorbate

Polyethylene glycol or polysorbate: PEG, macrogol or polysorbate; a rare cause of allergic reactions. 7 of 54 checked products list polyethylene glycol or polysorbate; 47 do not.

Does not list polyethylene glycol or polysorbate

Lists polyethylene glycol or polysorbate

Sevelamer without sorbitol or mannitol

Sorbitol or mannitol: sugar alcohols that can cause bloating or diarrhea in larger amounts. 18 of 54 checked products list sorbitol or mannitol; 36 do not.

Lists sorbitol or mannitol

At the pharmacy counter

How to use this at the pharmacy counter

  1. 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.
  2. 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.
  3. 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.
  4. 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.
Ask Dr. Staiger which Sevelamer product suits you →

Common questions about Sevelamer inactive ingredients

Is Sevelamer gluten-free?
This page cannot certify any Sevelamer product gluten-free; it reports what each label declares. Of the 54 products checked, none lists a wheat, barley, rye or gluten ingredient, and none lists a starch without a stated source. If you have celiac disease, ask the manufacturer's medical information line for a written gluten statement for the lot you have.
Does Sevelamer contain lactose?
4 of 54 checked Sevelamer products list lactose; 50 do not: Amneal (800 mg tablet), Amneal Pharmaceuticals of New York (800 mg oral suspension and 2400 mg oral suspension), Atlantic Biologicals (800 mg tablet) and Aurobindo (800 mg oral suspension, 400 mg tablet and 800 mg tablet) and 28 other companies. The lactose in a tablet or capsule is a small amount, but people with a milk allergy or a strong intolerance often prefer a version that does not list it.
Does Sevelamer contain soy?
3 of 54 checked Sevelamer products list a soy ingredient (soybean oil or soy lecithin); 51 do not: Amneal (800 mg tablet), Amneal Pharmaceuticals of New York (800 mg oral suspension and 2400 mg oral suspension), Atlantic Biologicals (800 mg tablet) and Aurobindo (800 mg oral suspension, 400 mg tablet and 800 mg tablet) and 28 other companies. Soy lecithin is the usual form and the amount is small, but people with a soy allergy often prefer a version that does not list it.
Is there a dye-free Sevelamer?
No checked Sevelamer product lists a synthetic dye (an FD&C or D&C colorant) on its label. Colorants often differ by strength within one company's line, so compare the lists above strength by strength.
Does Sevelamer contain gelatin?
No checked Sevelamer product lists gelatin on its label. Gelatin is usually bovine or porcine and the label rarely says which; for kosher, halal or vegetarian needs, ask the manufacturer.
Why do the inactive ingredients differ between manufacturers?
A generic must match the brand's active ingredient, strength, dose form and how it is absorbed; its fillers, binders, coatings and colorants are the manufacturer's own choice. That is why one Sevelamer product can list lactose and a dye while another from a different company lists neither.
Can my pharmacy give me a specific manufacturer's version?
Often, if you ask before the prescription is filled: many pharmacies order from wholesalers that carry several companies' versions and can request a particular one. Some pharmacies buy a generic from one contracted source only, and a few insurance plans cover only certain NDCs, so ask the pharmacist to check. Give them the NDC from this page; the company name alone is often enough.
How current is this list?
The products are the ones in the FDA's current NDC directory as of October 5, 2026, and each inactive-ingredient list is the manufacturer's FDA label as our label sync last read it. Formulations change, so check the label on your own bottle and ask your pharmacist if a refill looks different.

Sources: the products are the finished Sevelamer products in the FDA's current NDC directory (openFDA), as of October 5, 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 Sevelamer guide