Inactive ingredients by manufacturer

Sodium Bicarbonate inactive ingredients by manufacturer

Wondering whether your Sodium Bicarbonate 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 Sodium Bicarbonate 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 59 of the 89 current Sodium Bicarbonate products on the market today, from 54 companies listing it with the FDA, and lined them up side by side. 18 are still being read and will appear on a later visit. 5 labels have no inactive-ingredient list we could read, so those products cannot be compared. 7 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 Sodium Bicarbonate? 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 Sodium Bicarbonate products list lactose, a gluten source, soy, dyes or gelatin?

  1. LactoseNo checked product

    No checked Sodium Bicarbonate product lists lactose.

  2. Wheat or gluten sourceNo checked product

    No checked Sodium Bicarbonate product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Sodium Bicarbonate product lists soy.

  4. Synthetic dyesNo checked product

    No checked Sodium Bicarbonate product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Sodium Bicarbonate product lists gelatin.

Also listed by some products: Corn 5 of 59 Alcohol 1 of 59 PEG or polysorbate 2 of 59

Find a version without it

Every current Sodium Bicarbonate product and what its label lists

Hide products that list:

ProductListsInactive ingredients on the label
78271 1 product
5 g/25 g ointment or gel topical creamNDC 78271-0041-01 None of these listed
Show 10 ingredients

GLYCERYL CAPRYLATE, GLYCERYL MONOUNDECYLENATE, HONEY, PHENOXYETHANOL, PICEA ABIES LEAF OIL, POLYGLYCERYL-3 RICINOLEATE, PROPANEDIOL, SODIUM BENZOATE, WATER, XANTHAN GUM
A-S Medication Solutions 2 products
84 mg/mL injectionNDC 50090-0530-00 None of these listed
Show 3 ingredients

CARBON DIOXIDE, NITROGEN, WATER
84 mg/mL injectionNDC 50090-6813-00 None of these listed
Show 1 ingredient

WATER
Advanced Rx LLC 1 product
650 mg tabletNDC 80513-0611-02 Still being read Not read yet
Adventure Ready Brands 1 product
50 mg/1000 mL topical solutionNDC 44224-1040-00 Still being read Not read yet
Amneal Pharmaceuticals Private Limited 2 products
12.6 mg/mL injectionNDC 80830-2613-02 None of these listed
Show 2 ingredients

CARBON DIOXIDE, WATER
84 mg/mL injectionNDC 80830-2305-02 Still being read Not read yet
Anthea Pharma Private Limited 1 product
84 mg/mL injectionNDC 83854-0001-20 None of these listed
Show 3 ingredients

CARBON DIOXIDE, NITROGEN, WATER
Aphena Pharma Solutions - Tennessee, LLC 2 products
650 mg tabletNDC 71610-0669-53 None of these listed
Show 5 ingredients

CELLULOSE, MICROCRYSTALLINE, CROSCARMELLOSE SODIUM, SILICON DIOXIDE, STEARIC ACID, TALC
650 mg tabletNDC 43353-0162-53 None of these listed
Show 3 ingredients

CROSCARMELLOSE SODIUM, MICROCRYSTALLINE CELLULOSE, STEARIC ACID
Apnar Pharma Lp 1 product
650 mg tabletNDC 24689-0137-01 Still being read Not read yet
Baxter Healthcare Corporation 1 product
12.6 mg/mL injectionNDC 00338-0822-10 None of these listed
Show 2 ingredients

CARBON DIOXIDE, WATER
Bryant Ranch Prepack 2 products
84 mg/mL injectionNDC 72162-2314-02 None of these listed
Show 1 ingredient

WATER
650 mg tabletNDC 63629-8775-01 Corn-derived
Show 2 ingredients

CORN OIL, MICROCRYSTALLINE CELLULOSE
Cardinal Health 107, LLC 2 products
650 mg tabletNDC 55154-6754-00 Still being read Not read yet
650 mg tabletNDC 55154-4324-00 Still being read Not read yet
Church & Dwight Co., Inc. 1 product
1 g/g oral powderNDC 10237-0591-01 No inactive-ingredient list on the label No list we could read
CitraGen Pharmaceuticals Inc. 2 products
325 mg tabletNDC 70369-0002-01 None of these listed
Show 2 ingredients

CELLULOSE, MICROCRYSTALLINE, HYDROGENATED COTTONSEED OIL
650 mg tabletNDC 70369-0001-01 Still being read Not read yet
Civica 1 product
84 mg/mL injectionNDC 72572-0740-20 None of these listed
Show 1 ingredient

WATER
Cosmuses Cosmetics (Ningbo) Co., Ltd. 2 products
0.05 g ointment or gel topical creamNDC 82953-0019-01 Still being read Not read yet
5 g/100 g ointment or gel topical creamNDC 82953-0020-01 None of these listed
Show 13 ingredients

ALOE VERA LEAF, BUTYLATED HYDROXYTOLUENE, CETETH-25, CETOSTEARYL ALCOHOL, EDETATE DISODIUM, GLYCERIN, GLYCERYL MONOSTEARATE, METHYLPARABEN, MINERAL OIL, PHENOXYETHANOL, PROPYLPARABEN, WATER, YELLOW WAX
DLC Laboratories, Inc. 1 product
2.6 g/2.6 g oral powderNDC 24286-1537-07 Label gives only a general paragraph, not compared See the product page
Dlc Laboratories, Inc. 1 product
525 mg/15 mL oral solutionNDC 24286-1523-04 Alcohol (ethanol)
Show 5 ingredients

ALCOHOL, GLYCERIN, PEPPERMINT, RHUBARB, WATER
Evi Labs 4 products
315 mg/g oral powderNDC 84178-0050-01 Label gives only a general paragraph, not compared See the product page
315 mg/g oral powderNDC 84178-0105-02 Label gives only a general paragraph, not compared See the product page
315 mg/g oral powderNDC 84178-0106-01 Label gives only a general paragraph, not compared See the product page
616 mg/g oral powderNDC 84178-0104-01 Label gives only a general paragraph, not compared See the product page
Exela Pharma Sciences, LLC 6 products
42 mg/mL injectionNDC 51754-5012-04 Still being read Not read yet
75 mg/mL injectionNDC 51754-5002-05 None of these listed
Show 1 ingredient

WATER
84 mg/mL injectionNDC 51754-5001-04 None of these listed
Show 1 ingredient

WATER
84 mg/mL injectionNDC 51754-5011-04 None of these listed
Show 1 ingredient

WATER
84 mg/mL injectionNDC 51754-8020-04 None of these listed
Show 1 ingredient

WATER
84 mg/mL injectionNDC 51754-8888-04 Still being read Not read yet
Fresenius Kabi USA, LLC 2 products
42 mg/mL injectionNDC 63323-0083-05 Still being read Not read yet
84 mg/mL injectionNDC 63323-0089-50 None of these listed
Show 2 ingredients

CARBON DIOXIDE, WATER
Gendose Pharmaceuticals, LLC 1 product
650 mg tabletNDC 77333-0829-10 None of these listed
Show 2 ingredients

MICROCRYSTALLINE CELLULOSE, STEARIC ACID
Glenmark Pharmaceuticals Inc., USA 1 product
84 mg/mL injectionNDC 68462-0951-65 None of these listed
Show 3 ingredients

CARBON DIOXIDE, NITROGEN, WATER
Graxcell Pharmaceutical, Llc 1 product
650 mg tabletNDC 70795-1190-00 Corn-derived
Show 2 ingredients

MINERAL OIL, STARCH, CORN
Henry Schein, Inc. 2 products
42 mg/mL injectionNDC 00404-9951-05 None of these listed
Show 1 ingredient

WATER
84 mg/mL injectionNDC 00404-9980-50 None of these listed
Show 2 ingredients

CARBON DIOXIDE, WATER
HF Acquisition Co LLC, DBA HealthFirst 5 products
42 mg/mL injectionNDC 51662-1400-01 None of these listed
Show 2 ingredients

CARBON DIOXIDE, WATER
42 mg/mL injectionNDC 51662-1497-01 None of these listed
Show 1 ingredient

WATER
84 mg/mL injectionNDC 51662-1383-01 No inactive-ingredient list on the label No list we could read
84 mg/mL injectionNDC 51662-1255-01 None of these listed
Show 1 ingredient

WATER
84 mg/mL injectionNDC 51662-1573-01 Still being read Not read yet
Hospira, Inc. 3 products
42 mg/mL injectionNDC 00409-5555-01 None of these listed
Show 1 ingredient

WATER
84 mg/mL injectionNDC 00409-6625-14 None of these listed
Show 3 ingredients

CARBON DIOXIDE, NITROGEN, WATER
84 mg/mL injectionNDC 00409-6637-14 None of these listed
Show 1 ingredient

WATER
Humco Holding Group, Inc 1 product
1000 mg/g oral powderNDC 00802-2685-94 None of these listed
Show 1 ingredient

WATER
Humco Holding Group, Inc. 1 product
1000 mg/g oral powderNDC 00395-2685-01 None of these listed
Show 1 ingredient

WATER
International Medication Systems, Limited 1 product
84 mg/mL injectionNDC 76329-3352-01 No inactive-ingredient list on the label No list we could read
Lotus Brands, Inc. 2 products
25 mg/mL oral solutionNDC 76328-0221-01 Polyethylene glycol or polysorbate
Show 27 ingredients

ALOE VERA LEAF, ANETHOLE, BASIL OIL, BERGAMOT OIL, CHINESE CINNAMON OIL, CINNAMON LEAF OIL, CITRUS PARADISI SEED, CITRUS X LIMON SEED OIL, CLOVE OIL, ECHINACEA PURPUREA WHOLE, FENNEL OIL, GLYCERIN, GOLDENSEAL, LAVENDER OIL, MENTHOL, UNSPECIFIED FORM, ORANGE OIL, COLD PRESSED, PELARGONIUM GRAVEOLENS FLOWER OIL, PEPPERMINT OIL, POLYSORBATE 20, ROSA X DAMASCENA FLOWER OIL, ROSEMARY OIL, STAR ANISE OIL, STEVIA REBAUDIUNA LEAF, SULFATED CASTOR OIL, UBIDECARENONE, WATER, WITCH HAZEL
25 mg/mL oral solutionNDC 76328-0223-01 Polyethylene glycol or polysorbate
Show 25 ingredients

ALOE VERA LEAF, ANETHOLE, BASIL OIL, BERGAMOT OIL, CITRUS PARADISI SEED, CITRUS X LIMON SEED OIL, Clove Oil, ECHINACEA PURPUREA WHOLE, FENNEL OIL, GLYCERIN, GOLDENSEAL, LAVENDER OIL, MENTHOL, UNSPECIFIED FORM, ORANGE OIL, COLD PRESSED, PELARGONIUM GRAVEOLENS FLOWER OIL, PEPPERMINT OIL, POLYSORBATE 20, ROSA X DAMASCENA FLOWER OIL, ROSEMARY OIL, STAR ANISE OIL, STEVIA REBAUDIUNA LEAF, SULFATED CASTOR OIL, UBIDECARENONE, WATER, WITCH HAZEL
Major Pharmaceuticals 1 product
650 mg tabletNDC 00904-7261-61 None of these listed
Show 5 ingredients

CROSCARMELLOSE SODIUM, MICROCRYSTALLINE CELLULOSE, SILICON DIOXIDE, STEARIC ACID, TALC
Medical Purchasing Solutions, LLC 5 products
84 mg/mL injectionNDC 71872-7097-01 Still being read Not read yet
84 mg/mL injectionNDC 71872-7247-01 None of these listed
Show 3 ingredients

CARBON DIOXIDE, NITROGEN, WATER
84 mg/mL injectionNDC 71872-7266-01 None of these listed
Show 1 ingredient

WATER
84 mg/mL injectionNDC 71872-7310-01 Still being read Not read yet
84 mg/mL injectionNDC 71872-7371-01 None of these listed
Show 1 ingredient

WATER
Medical Purchasing Solutions, LLC. 1 product
84 mg/mL injectionNDC 71872-7376-01 None of these listed
Show 3 ingredients

CARBON DIOXIDE, NITROGEN, WATER
Menper Distributors, Inc. 1 product
525 mg/15 mL oral solutionNDC 53145-0300-08 Still being read Not read yet
Menper Distributors Inc. 1 product
2.616 g/2.616 g oral powderNDC 53145-0390-04 None of these listed
Show 1 ingredient

SODIUM CATION
Milla Pharmaceuticals Inc. 1 product
84 mg/mL injectionNDC 71357-0004-10 None of these listed
Show 2 ingredients

CARBON DIOXIDE, WATER
NCS HealthCare of KY, LLC dba Vangard Labs 1 product
650 mg tabletNDC 00615-8641-39 None of these listed
Show 5 ingredients

CELLULOSE, MICROCRYSTALLINE, CROSCARMELLOSE SODIUM, SILICON DIOXIDE, STEARIC ACID, TALC
Omnivium Pharmaceuticals Llc. 1 product
84 mg/mL injectionNDC 81665-0200-05 None of these listed
Show 1 ingredient

WATER
Pharmadel LLC 1 product
2.6 g/2.6 g oral powderNDC 55758-0319-04 Label gives only a general paragraph, not compared See the product page
Pharma Nobis, LLC 1 product
1000 mg/g oral powderNDC 82645-0904-01 None of these listed
Show 1 ingredient

WATER
ProPharma Distribution 2 products
84 mg/mL injectionNDC 84549-0352-01 No inactive-ingredient list on the label No list we could read
84 mg/mL injectionNDC 84549-0050-03 None of these listed
Show 1 ingredient

WATER
Reliable 1 Laboratories LLC 1 product
648 mg tabletNDC 69618-0034-10 None of these listed
Show 3 ingredients

CELLULOSE, MICROCRYSTALLINE, CROSCARMELLOSE SODIUM, STEARIC ACID
Remedyrepack Inc. 1 product
84 mg/mL injectionNDC 70518-4158-00 No inactive-ingredient list on the label No list we could read
Richmond Pharmaceuticals, Inc. 2 products
325 mg tabletNDC 54738-0035-03 None of these listed
Show 5 ingredients

CELLULOSE, MICROCRYSTALLINE, CROSCARMELLOSE SODIUM, SILICON DIOXIDE, STEARIC ACID, TALC
650 mg tabletNDC 54738-0020-03 Still being read Not read yet
Rising Pharma Holdings, Inc. 1 product
650 mg tabletNDC 64980-0528-10 Corn-derived
Show 2 ingredients

CORN OIL, MICROCRYSTALLINE CELLULOSE
Rugby Laboratories 2 products
325 mg tabletNDC 00536-1046-10 None of these listed
Show 5 ingredients

CELLULOSE, MICROCRYSTALLINE, CROSCARMELLOSE SODIUM, SILICON DIOXIDE, STEARIC ACID, TALC
650 mg tabletNDC 00536-1047-10 None of these listed
Show 5 ingredients

CELLULOSE, MICROCRYSTALLINE, CROSCARMELLOSE SODIUM, SILICON DIOXIDE, STEARIC ACID, TALC
Steriscience Specialties Private Limited 1 product
84 mg/mL injectionNDC 82449-0000-05 None of these listed
Show 1 ingredient

WATER
Sun Pharmaceutical Industries Limited 1 product
84 mg/mL injectionNDC 70095-0050-03 None of these listed
Show 1 ingredient

WATER
Tender Corporation d/b/a Adventure Ready Brands 3 products
1.04 g/20 g ointment or gel topical creamNDC 44224-1117-02 None of these listed
Show 10 ingredients

.ALPHA.-TOCOPHEROL ACETATE, ALOE VERA LEAF, DIMETHICONE 350, EUCALYPTUS OIL, OLETH-10 PHOSPHATE, OLETH-3 PHOSPHATE, SODIUM HYDROXIDE, TEA TREE OIL, WATER, WHITE WAX
1.04 g/20 g ointment or gel topical creamNDC 44224-2421-01 Still being read Not read yet
0.7 g/14 g topical solutionNDC 44224-1103-02 None of these listed
Show 3 ingredients

AMMONIA, GLYCERIN, WATER
Twin Med Llc 3 products
325 mg tabletNDC 55681-0072-02 Corn-derived
Show 2 ingredients

MINERAL OIL, STARCH, CORN
325 mg tabletNDC 55681-0307-02 Corn-derived
Show 2 ingredients

MINERAL OIL, STARCH, CORN
650 mg tabletNDC 55681-0332-10 Still being read Not read yet
Vitamex USA, Corp 1 product
2.6 g/2.6 g oral powderNDC 69469-0100-04 Label gives only a general paragraph, not compared See the product page
Wenzhou Yuyuan Pharmaceutical Co., Ltd. 1 product
5 g/100 mL topical solutionNDC 87786-0030-01 None of these listed
Show 3 ingredients

AMMONIA, GLYCERIN, WATER
Westminster Pharmaceuticals, LLC 1 product
650 mg tabletNDC 69367-0258-10 None of these listed
Show 2 ingredients

MICROCRYSTALLINE CELLULOSE, STEARIC ACID
World Perfumes Inc 1 product
2.6 g/2.6 g oral powderNDC 10095-0100-01 None of these listed
Show 1 ingredient

BICARBONATE ION

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.

Sodium Bicarbonate without corn-derived ingredients

Corn-derived: corn starch, maize or corn syrup; a concern with corn allergy. 5 of 59 checked products list corn-derived ingredients; 54 do not.

Does not list corn-derived ingredients

Lists corn-derived ingredients

Sodium Bicarbonate without alcohol (ethanol)

Alcohol (ethanol): mostly in liquids; a concern in alcohol recovery, for children, or with disulfiram or metronidazole. 1 of 59 checked products list alcohol (ethanol); 58 do not.

Does not list alcohol (ethanol)

Lists alcohol (ethanol)

Sodium Bicarbonate without polyethylene glycol or polysorbate

Polyethylene glycol or polysorbate: PEG, macrogol or polysorbate; a rare cause of allergic reactions. 2 of 59 checked products list polyethylene glycol or polysorbate; 57 do not.

Does not list polyethylene glycol or polysorbate

Lists polyethylene glycol or polysorbate

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 Sodium Bicarbonate product suits you →

Common questions about Sodium Bicarbonate inactive ingredients

Is Sodium Bicarbonate gluten-free?
This page cannot certify any Sodium Bicarbonate product gluten-free; it reports what each label declares. Of the 59 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 Sodium Bicarbonate contain lactose?
No checked Sodium Bicarbonate product lists lactose on its label. 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 Sodium Bicarbonate contain soy?
No checked Sodium Bicarbonate product lists a soy ingredient (soybean oil or soy lecithin) on its label. 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 Sodium Bicarbonate?
No checked Sodium Bicarbonate 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 Sodium Bicarbonate contain gelatin?
No checked Sodium Bicarbonate 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 Sodium Bicarbonate 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 Sodium Bicarbonate 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 Sodium Bicarbonate guide