Hyoscyamine inactive ingredients by manufacturer
Wondering whether your Hyoscyamine 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 Hyoscyamine 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 53 of the 54 current Hyoscyamine products on the market today, from 23 companies listing it with the FDA, and lined them up side by side. 1 label has no inactive-ingredient list we could read, so that product cannot be compared.
Ask about your bottle
Is there something in your Hyoscyamine? 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 Hyoscyamine products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseDiffers by manufacturer
27 of 53 checked products list lactose; 26 do not. See the products
-
Wheat or gluten sourceNo checked product
No checked Hyoscyamine product lists a wheat or gluten source.
-
SoyNo checked product
No checked Hyoscyamine product lists soy.
-
Synthetic dyesDiffers by manufacturer
29 of 53 checked products list synthetic dyes; 24 do not. See the products
-
GelatinNo checked product
No checked Hyoscyamine product lists gelatin.
Also listed by some products: Corn 24 of 53 Alcohol 6 of 53 Sorbitol or mannitol 42 of 53 Sugar 6 of 53
Find a version without it
Every current Hyoscyamine product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Acella Pharmaceuticals, LLC 3 products | ||
| 0.125 mg orally disintegrating tabletNDC 42192-0338-01 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 7 ingredientsD&C YELLOW NO. 10, FD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| 0.125 mg sublingual tabletNDC 42192-0339-01 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 7 ingredientsD&C YELLOW NO. 10, FD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| 0.125 mg tabletNDC 42192-0340-01 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 7 ingredientsD&C YELLOW NO. 10, FD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| ANI Pharmaceuticals, Inc. 4 products | ||
| 0.375 mg extended-release tabletNDC 62559-0423-01 | None of these listed |
Show 4 ingredientsHYDROXYPROPYL CELLULOSE (1600000 WAMW), MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, SILICON DIOXIDE |
| 0.125 mg orally disintegrating tabletNDC 62559-0422-01 | Sorbitol or mannitol |
Show 5 ingredientsCROSPOVIDONE (120 .MU.M), MAGNESIUM STEARATE, MANNITOL, SILICON DIOXIDE, SORBITOL |
| 0.125 mg sublingual tabletNDC 62559-0424-01 | Sorbitol or mannitol |
Show 5 ingredientsCROSPOVIDONE (120 .MU.M), MAGNESIUM STEARATE, MANNITOL, SILICON DIOXIDE, SORBITOL |
| 0.125 mg tabletNDC 62559-0421-01 | None of these listed |
Show 3 ingredientsCROSPOVIDONE (120 .MU.M), MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE |
| Atlantic Biologicals Corp. 2 products | ||
| 0.125 mg/5 mL oral solutionNDC 17856-0511-02 | Synthetic dyes Alcohol (ethanol) Sorbitol or mannitol Sugar (sucrose, dextrose) |
Show 10 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, FD&C RED NO. 40, FD&C YELLOW NO. 6, GLYCERIN, SODIUM BENZOATE, SODIUM CITRATE, UNSPECIFIED FORM, SORBITOL, SUCROSE, WATER |
| 0.125 mg/5 mL oral solutionNDC 17856-0514-05 | Synthetic dyes Alcohol (ethanol) Sorbitol or mannitol Sugar (sucrose, dextrose) |
Show 10 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, FD&C RED NO. 40, FD&C YELLOW NO. 6, GLYCERIN, SODIUM BENZOATE, SODIUM CITRATE, SORBITOL, SUCROSE, WATER |
| BPI Labs LLC 1 product | ||
| 0.5 mg/mL injectionNDC 54288-0111-05 | None of these listed |
Show 1 ingredientWATER |
| Bryant Ranch Prepack 6 products | ||
| 0.125 mg sublingual tabletNDC 71335-1159-00 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 7 ingredientsD&C YELLOW NO. 10, FD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| 0.125 mg tabletNDC 72162-1939-01 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 6 ingredientsFD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| 0.125 mg tabletNDC 71335-1647-00 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 6 ingredientsFD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| 0.125 mg tabletNDC 72162-1940-01 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 6 ingredientsFD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| 0.125 mg tabletNDC 72162-1941-01 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 7 ingredientsD&C YELLOW NO. 10, FD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| 0.125 mg tabletNDC 63629-5911-01 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 7 ingredientsD&C YELLOW NO. 10, FD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| Chartwell RX, LLC 6 products | ||
| 0.375 mg extended-release tabletNDC 62135-0860-60 | None of these listed |
Show 4 ingredientsHYDROXYPROPYL CELLULOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, SILICON DIOXIDE |
| 0.125 mg orally disintegrating tabletNDC 62135-0858-12 | Sorbitol or mannitol |
Show 6 ingredientsCROSPOVIDONE, UNSPECIFIED, MAGNESIUM STEARATE, MANNITOL, SILICON DIOXIDE, SODIUM STEARYL FUMARATE, SORBITOL |
| 0.125 mg/5 mL oral solutionNDC 62135-0511-47 | Synthetic dyes Alcohol (ethanol) Sorbitol or mannitol Sugar (sucrose, dextrose) |
Show 11 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, FD&C RED NO. 40, FD&C YELLOW NO. 6, GLYCERIN, LEMON, SODIUM BENZOATE, SODIUM CITRATE, SORBITOL, SUCROSE, WATER |
| 0.125 mg/mL oral solutionNDC 62135-0513-52 | Synthetic dyes Alcohol (ethanol) Sorbitol or mannitol Sugar (sucrose, dextrose) |
Show 11 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, FD&C RED NO. 40, FD&C YELLOW NO. 6, GLYCERIN, LEMON, SODIUM BENZOATE, SODIUM CITRATE, SORBITOL, SUCROSE, WATER |
| 0.125 mg sublingual tabletNDC 62135-0859-12 | Sorbitol or mannitol |
Show 6 ingredientsCROSPOVIDONE, UNSPECIFIED, MAGNESIUM STEARATE, MANNITOL, SILICON DIOXIDE, SODIUM STEARYL FUMARATE, SORBITOL |
| 0.125 mg tabletNDC 62135-0512-12 | None of these listed |
Show 4 ingredientsCROSPOVIDONE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, SILICON DIOXIDE |
| Direct_Rx 1 product | ||
| 0.125 mg sublingual tabletNDC 72189-0666-30 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 7 ingredientsD&C YELLOW NO. 10, FD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| Granulation Technology, Inc. 3 products | ||
| 0.125 mg orally disintegrating tabletNDC 63561-0197-01 | Sorbitol or mannitol |
Show 5 ingredientsCROSPOVIDONE (15 MPA.S AT 5%), MAGNESIUM STEARATE, MANNITOL, MICROCRYSTALLINE CELLULOSE, SILICON DIOXIDE |
| 0.125 mg sublingual tabletNDC 63561-0202-01 | Sorbitol or mannitol |
Show 5 ingredientsCROSPOVIDONE (15 MPA.S AT 5%), MAGNESIUM STEARATE, MANNITOL, MICROCRYSTALLINE CELLULOSE, SILICON DIOXIDE |
| 0.125 mg tabletNDC 63561-0203-01 | Sorbitol or mannitol |
Show 5 ingredientsCROSPOVIDONE (120 .MU.M), MAGNESIUM STEARATE, MANNITOL, MICROCRYSTALLINE CELLULOSE, SILICON DIOXIDE |
| Lannett Company, Inc. 2 products | ||
| 0.125 mg/5 mL oral solutionNDC 54838-0511-80 | Synthetic dyes Alcohol (ethanol) Sorbitol or mannitol Sugar (sucrose, dextrose) |
Show 10 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, FD&C RED NO. 40, FD&C YELLOW NO. 6, GLYCERIN, SODIUM BENZOATE, SODIUM CITRATE, SORBITOL, SUCROSE, WATER |
| 0.125 mg/mL oral solutionNDC 54838-0506-15 | Synthetic dyes Alcohol (ethanol) Sorbitol or mannitol Sugar (sucrose, dextrose) |
Show 10 ingredientsALCOHOL, ANHYDROUS CITRIC ACID, FD&C RED NO. 40, FD&C YELLOW NO. 6, GLYCERIN, SODIUM BENZOATE, SODIUM CITRATE, SORBITOL, SUCROSE, WATER |
| Larken Laboratories, Inc. 2 products | ||
| 0.125 mg sublingual tabletNDC 68047-0253-01 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 7 ingredientsD&C YELLOW NO. 10, FD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| 0.125 mg tabletNDC 68047-0252-01 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 7 ingredientsD&C YELLOW NO. 10, FD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| Laser Pharmaceuticals, LLC 1 product | ||
| 0.375 mg extended-release tabletNDC 16477-0738-01 | Lactose |
Show 6 ingredientsANHYDROUS DIBASIC CALCIUM PHOSPHATE, CELLULOSE, MICROCRYSTALLINE, ETHYLCELLULOSE (10 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, STEARIC ACID |
| Mylan Pharmaceuticals Inc. 1 product | ||
| 0.375 mg extended-release tabletNDC 51525-0115-01 | No inactive-ingredient list on the label | No list we could read |
| NCS HealthCare of KY, LLC dba Vangard Labs 2 products | ||
| 0.125 mg sublingual tabletNDC 00615-8554-39 | Sorbitol or mannitol |
Show 5 ingredientsCROSPOVIDONE, MAGNESIUM STEARATE, MANNITOL, SILICON DIOXIDE, SORBITOL |
| 0.125 mg tabletNDC 00615-8537-39 | None of these listed |
Show 3 ingredientsCROSPOVIDONE (120 .MU.M), MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE |
| Northwind Health Company, LLC 2 products | ||
| 0.125 mg tabletNDC 51655-0845-52 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 7 ingredientsD&C YELLOW NO. 10, FD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| 0.125 mg tabletNDC 51655-0764-52 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 6 ingredientsFD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| Patrin Pharma, Inc. 4 products | ||
| 0.375 mg extended-release tabletNDC 39328-0052-10 | None of these listed |
Show 4 ingredientsHYDROXYPROPYL CELLULOSE (1600000 WAMW), Magnesium Stearate, Microcrystalline Cellulose, SILICON DIOXIDE |
| 0.125 mg orally disintegrating tabletNDC 39328-0049-10 | Sorbitol or mannitol |
Show 4 ingredientsCROSPOVIDONE, UNSPECIFIED, Magnesium Stearate, Mannitol, SILICON DIOXIDE |
| 0.125 mg sublingual tabletNDC 39328-0051-10 | Sorbitol or mannitol |
Show 4 ingredientsCROSPOVIDONE, UNSPECIFIED, Magnesium Stearate, Mannitol, SILICON DIOXIDE |
| 0.125 mg tabletNDC 39328-0050-10 | Sorbitol or mannitol |
Show 4 ingredientsCROSPOVIDONE, UNSPECIFIED, Magnesium Stearate, Mannitol, SILICON DIOXIDE |
| PD-Rx Pharmaceuticals, Inc. 1 product | ||
| 0.125 mg orally disintegrating tabletNDC 72789-0563-01 | Sorbitol or mannitol |
Show 5 ingredientsCROSPOVIDONE (15 MPA.S AT 5%), MAGNESIUM STEARATE, MANNITOL, MICROCRYSTALLINE CELLULOSE, SILICON DIOXIDE |
| Proficient Rx LP 1 product | ||
| 0.125 mg tabletNDC 82804-0965-30 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 6 ingredientsFD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| PureTek Corporation 1 product | ||
| 0.125 mg tabletNDC 59088-0150-54 | Lactose |
Show 5 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, SODIUM STARCH GLYCOLATE TYPE A POTATO, STEARIC ACID |
| QPharma, Inc. 1 product | ||
| 0.125 mg tabletNDC 42708-0183-56 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 7 ingredientsD&C YELLOW NO. 10, FD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| Redpharm Drug 1 product | ||
| 0.125 mg sublingual tabletNDC 67296-2300-01 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 7 ingredientsD&C YELLOW NO. 10, FD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| Remedyrepack Inc. 2 products | ||
| 0.125 mg tabletNDC 70518-4436-00 | None of these listed |
Show 3 ingredientsCROSPOVIDONE, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE |
| 0.125 mg tabletNDC 70518-3847-00 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 7 ingredientsD&C YELLOW NO. 10, FD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| Viatris Specialty LLC 4 products | ||
| 0.125 mg chewable tabletNDC 68220-0118-10 | Lactose Corn-derived Sorbitol or mannitol |
Show 6 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, PEPPERMINT, STARCH, CORN, STEARIC ACID |
| 0.375 mg extended-release tabletNDC 68220-0115-10 | Lactose |
Show 6 ingredientsANHYDROUS DIBASIC CALCIUM PHOSPHATE, ETHYLCELLULOSE, UNSPECIFIED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, STEARIC ACID |
| 0.125 mg orally disintegrating tabletNDC 68220-0113-10 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 6 ingredientsFD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| 0.125 mg tabletNDC 68220-0112-10 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 6 ingredientsFD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| Westminster Pharmaceuticals, LLC 3 products | ||
| 0.125 mg orally disintegrating tabletNDC 69367-0679-01 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 7 ingredientsD&C YELLOW NO. 10, FD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| 0.125 mg tabletNDC 69367-0678-01 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 6 ingredientsFD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
| 0.125 mg tabletNDC 69367-0677-01 | Lactose Corn-derived Synthetic dyes Sorbitol or mannitol |
Show 6 ingredientsFD&C BLUE NO. 1, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, STEARIC ACID |
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.
Hyoscyamine without lactose
Lactose: milk sugar; a concern with lactose intolerance or a milk allergy. 27 of 53 checked products list lactose; 26 do not.
Does not list lactose
- ANI: 0.375 mg extended-release tablet, 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- Atlantic Biologicals: 0.125 mg/5 mL oral solution (NDC 17856-0511-02), 0.125 mg/5 mL oral solution (NDC 17856-0514-05)
- BPI: 0.5 mg/mL injection
- Chartwell RX: 0.375 mg extended-release tablet, 0.125 mg orally disintegrating tablet, 0.125 mg/5 mL oral solution, 0.125 mg/mL oral solution, 0.125 mg sublingual tablet, 0.125 mg tablet
- Granulation Technology: 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- Lannett: 0.125 mg/5 mL oral solution, 0.125 mg/mL oral solution
- NCS HealthCare of KY, LLC dba Vangard: 0.125 mg sublingual tablet, 0.125 mg tablet
- Patrin: 0.375 mg extended-release tablet, 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- PD-Rx: 0.125 mg orally disintegrating tablet
- Remedyrepack: 0.125 mg tablet
Lists lactose
- Acella: 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- Bryant Ranch Prepack: 0.125 mg sublingual tablet, 0.125 mg tablet (NDC 72162-1939-01), 0.125 mg tablet (NDC 71335-1647-00), 0.125 mg tablet (NDC 72162-1940-01), 0.125 mg tablet (NDC 72162-1941-01), 0.125 mg tablet (NDC 63629-5911-01)
- Direct_Rx: 0.125 mg sublingual tablet
- Larken: 0.125 mg sublingual tablet, 0.125 mg tablet
- Laser: 0.375 mg extended-release tablet
- Northwind Health: 0.125 mg tablet (NDC 51655-0845-52), 0.125 mg tablet (NDC 51655-0764-52)
- Proficient Rx: 0.125 mg tablet
- PureTek: 0.125 mg tablet
- QPharma: 0.125 mg tablet
- Redpharm Drug: 0.125 mg sublingual tablet
- Remedyrepack: 0.125 mg tablet
- Viatris Specialty: 0.125 mg chewable tablet, 0.375 mg extended-release tablet, 0.125 mg orally disintegrating tablet, 0.125 mg tablet
- Westminster: 0.125 mg orally disintegrating tablet, 0.125 mg tablet (NDC 69367-0678-01), 0.125 mg tablet (NDC 69367-0677-01)
Hyoscyamine without synthetic dyes
Synthetic dyes: FD&C or D&C colorants and their aluminum lakes. 29 of 53 checked products list synthetic dyes; 24 do not.
Does not list synthetic dyes
- ANI: 0.375 mg extended-release tablet, 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- BPI: 0.5 mg/mL injection
- Chartwell RX: 0.375 mg extended-release tablet, 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- Granulation Technology: 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- Laser: 0.375 mg extended-release tablet
- NCS HealthCare of KY, LLC dba Vangard: 0.125 mg sublingual tablet, 0.125 mg tablet
- Patrin: 0.375 mg extended-release tablet, 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- PD-Rx: 0.125 mg orally disintegrating tablet
- PureTek: 0.125 mg tablet
- Remedyrepack: 0.125 mg tablet
- Viatris Specialty: 0.125 mg chewable tablet, 0.375 mg extended-release tablet
Lists synthetic dyes
- Acella: 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- Atlantic Biologicals: 0.125 mg/5 mL oral solution (NDC 17856-0511-02), 0.125 mg/5 mL oral solution (NDC 17856-0514-05)
- Bryant Ranch Prepack: 0.125 mg sublingual tablet, 0.125 mg tablet (NDC 72162-1939-01), 0.125 mg tablet (NDC 71335-1647-00), 0.125 mg tablet (NDC 72162-1940-01), 0.125 mg tablet (NDC 72162-1941-01), 0.125 mg tablet (NDC 63629-5911-01)
- Chartwell RX: 0.125 mg/5 mL oral solution, 0.125 mg/mL oral solution
- Direct_Rx: 0.125 mg sublingual tablet
- Lannett: 0.125 mg/5 mL oral solution, 0.125 mg/mL oral solution
- Larken: 0.125 mg sublingual tablet, 0.125 mg tablet
- Northwind Health: 0.125 mg tablet (NDC 51655-0845-52), 0.125 mg tablet (NDC 51655-0764-52)
- Proficient Rx: 0.125 mg tablet
- QPharma: 0.125 mg tablet
- Redpharm Drug: 0.125 mg sublingual tablet
- Remedyrepack: 0.125 mg tablet
- Viatris Specialty: 0.125 mg orally disintegrating tablet, 0.125 mg tablet
- Westminster: 0.125 mg orally disintegrating tablet, 0.125 mg tablet (NDC 69367-0678-01), 0.125 mg tablet (NDC 69367-0677-01)
Hyoscyamine without corn-derived ingredients
Corn-derived: corn starch, maize or corn syrup; a concern with corn allergy. 24 of 53 checked products list corn-derived ingredients; 29 do not.
Does not list corn-derived ingredients
- ANI: 0.375 mg extended-release tablet, 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- Atlantic Biologicals: 0.125 mg/5 mL oral solution (NDC 17856-0511-02), 0.125 mg/5 mL oral solution (NDC 17856-0514-05)
- BPI: 0.5 mg/mL injection
- Chartwell RX: 0.375 mg extended-release tablet, 0.125 mg orally disintegrating tablet, 0.125 mg/5 mL oral solution, 0.125 mg/mL oral solution, 0.125 mg sublingual tablet, 0.125 mg tablet
- Granulation Technology: 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- Lannett: 0.125 mg/5 mL oral solution, 0.125 mg/mL oral solution
- Laser: 0.375 mg extended-release tablet
- NCS HealthCare of KY, LLC dba Vangard: 0.125 mg sublingual tablet, 0.125 mg tablet
- Patrin: 0.375 mg extended-release tablet, 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- PD-Rx: 0.125 mg orally disintegrating tablet
- PureTek: 0.125 mg tablet
- Remedyrepack: 0.125 mg tablet
- Viatris Specialty: 0.375 mg extended-release tablet
Lists corn-derived ingredients
- Acella: 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- Bryant Ranch Prepack: 0.125 mg sublingual tablet, 0.125 mg tablet (NDC 72162-1939-01), 0.125 mg tablet (NDC 71335-1647-00), 0.125 mg tablet (NDC 72162-1940-01), 0.125 mg tablet (NDC 72162-1941-01), 0.125 mg tablet (NDC 63629-5911-01)
- Direct_Rx: 0.125 mg sublingual tablet
- Larken: 0.125 mg sublingual tablet, 0.125 mg tablet
- Northwind Health: 0.125 mg tablet (NDC 51655-0845-52), 0.125 mg tablet (NDC 51655-0764-52)
- Proficient Rx: 0.125 mg tablet
- QPharma: 0.125 mg tablet
- Redpharm Drug: 0.125 mg sublingual tablet
- Remedyrepack: 0.125 mg tablet
- Viatris Specialty: 0.125 mg chewable tablet, 0.125 mg orally disintegrating tablet, 0.125 mg tablet
- Westminster: 0.125 mg orally disintegrating tablet, 0.125 mg tablet (NDC 69367-0678-01), 0.125 mg tablet (NDC 69367-0677-01)
Hyoscyamine without alcohol (ethanol)
Alcohol (ethanol): mostly in liquids; a concern in alcohol recovery, for children, or with disulfiram or metronidazole. 6 of 53 checked products list alcohol (ethanol); 47 do not.
Does not list alcohol (ethanol)
- Acella: 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- ANI: 0.375 mg extended-release tablet, 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- BPI: 0.5 mg/mL injection
- Bryant Ranch Prepack: 0.125 mg sublingual tablet, 0.125 mg tablet (NDC 72162-1939-01), 0.125 mg tablet (NDC 71335-1647-00), 0.125 mg tablet (NDC 72162-1940-01), 0.125 mg tablet (NDC 72162-1941-01), 0.125 mg tablet (NDC 63629-5911-01)
- Chartwell RX: 0.375 mg extended-release tablet, 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- Direct_Rx: 0.125 mg sublingual tablet
- Granulation Technology: 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- Larken: 0.125 mg sublingual tablet, 0.125 mg tablet
- Laser: 0.375 mg extended-release tablet
- NCS HealthCare of KY, LLC dba Vangard: 0.125 mg sublingual tablet, 0.125 mg tablet
- Northwind Health: 0.125 mg tablet (NDC 51655-0845-52), 0.125 mg tablet (NDC 51655-0764-52)
- Patrin: 0.375 mg extended-release tablet, 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- PD-Rx: 0.125 mg orally disintegrating tablet
- Proficient Rx: 0.125 mg tablet
- PureTek: 0.125 mg tablet
- QPharma: 0.125 mg tablet
- Redpharm Drug: 0.125 mg sublingual tablet
- Remedyrepack: 0.125 mg tablet (NDC 70518-4436-00), 0.125 mg tablet (NDC 70518-3847-00)
- Viatris Specialty: 0.125 mg chewable tablet, 0.375 mg extended-release tablet, 0.125 mg orally disintegrating tablet, 0.125 mg tablet
- Westminster: 0.125 mg orally disintegrating tablet, 0.125 mg tablet (NDC 69367-0678-01), 0.125 mg tablet (NDC 69367-0677-01)
Lists alcohol (ethanol)
- Atlantic Biologicals: 0.125 mg/5 mL oral solution (NDC 17856-0511-02), 0.125 mg/5 mL oral solution (NDC 17856-0514-05)
- Chartwell RX: 0.125 mg/5 mL oral solution, 0.125 mg/mL oral solution
- Lannett: 0.125 mg/5 mL oral solution, 0.125 mg/mL oral solution
Hyoscyamine without sorbitol or mannitol
Sorbitol or mannitol: sugar alcohols that can cause bloating or diarrhea in larger amounts. 42 of 53 checked products list sorbitol or mannitol; 11 do not.
Does not list sorbitol or mannitol
- ANI: 0.375 mg extended-release tablet, 0.125 mg tablet
- BPI: 0.5 mg/mL injection
- Chartwell RX: 0.375 mg extended-release tablet, 0.125 mg tablet
- Laser: 0.375 mg extended-release tablet
- NCS HealthCare of KY, LLC dba Vangard: 0.125 mg tablet
- Patrin: 0.375 mg extended-release tablet
- PureTek: 0.125 mg tablet
- Remedyrepack: 0.125 mg tablet
- Viatris Specialty: 0.375 mg extended-release tablet
Lists sorbitol or mannitol
- Acella: 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- ANI: 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet
- Atlantic Biologicals: 0.125 mg/5 mL oral solution (NDC 17856-0511-02), 0.125 mg/5 mL oral solution (NDC 17856-0514-05)
- Bryant Ranch Prepack: 0.125 mg sublingual tablet, 0.125 mg tablet (NDC 72162-1939-01), 0.125 mg tablet (NDC 71335-1647-00), 0.125 mg tablet (NDC 72162-1940-01), 0.125 mg tablet (NDC 72162-1941-01), 0.125 mg tablet (NDC 63629-5911-01)
- Chartwell RX: 0.125 mg orally disintegrating tablet, 0.125 mg/5 mL oral solution, 0.125 mg/mL oral solution, 0.125 mg sublingual tablet
- Direct_Rx: 0.125 mg sublingual tablet
- Granulation Technology: 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- Lannett: 0.125 mg/5 mL oral solution, 0.125 mg/mL oral solution
- Larken: 0.125 mg sublingual tablet, 0.125 mg tablet
- NCS HealthCare of KY, LLC dba Vangard: 0.125 mg sublingual tablet
- Northwind Health: 0.125 mg tablet (NDC 51655-0845-52), 0.125 mg tablet (NDC 51655-0764-52)
- Patrin: 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- PD-Rx: 0.125 mg orally disintegrating tablet
- Proficient Rx: 0.125 mg tablet
- QPharma: 0.125 mg tablet
- Redpharm Drug: 0.125 mg sublingual tablet
- Remedyrepack: 0.125 mg tablet
- Viatris Specialty: 0.125 mg chewable tablet, 0.125 mg orally disintegrating tablet, 0.125 mg tablet
- Westminster: 0.125 mg orally disintegrating tablet, 0.125 mg tablet (NDC 69367-0678-01), 0.125 mg tablet (NDC 69367-0677-01)
Hyoscyamine without sugar (sucrose or dextrose)
Sugar (sucrose, dextrose): A consideration in diabetes, mostly in liquids and chewables. 6 of 53 checked products list sugar (sucrose or dextrose); 47 do not.
Does not list sugar (sucrose or dextrose)
- Acella: 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- ANI: 0.375 mg extended-release tablet, 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- BPI: 0.5 mg/mL injection
- Bryant Ranch Prepack: 0.125 mg sublingual tablet, 0.125 mg tablet (NDC 72162-1939-01), 0.125 mg tablet (NDC 71335-1647-00), 0.125 mg tablet (NDC 72162-1940-01), 0.125 mg tablet (NDC 72162-1941-01), 0.125 mg tablet (NDC 63629-5911-01)
- Chartwell RX: 0.375 mg extended-release tablet, 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- Direct_Rx: 0.125 mg sublingual tablet
- Granulation Technology: 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- Larken: 0.125 mg sublingual tablet, 0.125 mg tablet
- Laser: 0.375 mg extended-release tablet
- NCS HealthCare of KY, LLC dba Vangard: 0.125 mg sublingual tablet, 0.125 mg tablet
- Northwind Health: 0.125 mg tablet (NDC 51655-0845-52), 0.125 mg tablet (NDC 51655-0764-52)
- Patrin: 0.375 mg extended-release tablet, 0.125 mg orally disintegrating tablet, 0.125 mg sublingual tablet, 0.125 mg tablet
- PD-Rx: 0.125 mg orally disintegrating tablet
- Proficient Rx: 0.125 mg tablet
- PureTek: 0.125 mg tablet
- QPharma: 0.125 mg tablet
- Redpharm Drug: 0.125 mg sublingual tablet
- Remedyrepack: 0.125 mg tablet (NDC 70518-4436-00), 0.125 mg tablet (NDC 70518-3847-00)
- Viatris Specialty: 0.125 mg chewable tablet, 0.375 mg extended-release tablet, 0.125 mg orally disintegrating tablet, 0.125 mg tablet
- Westminster: 0.125 mg orally disintegrating tablet, 0.125 mg tablet (NDC 69367-0678-01), 0.125 mg tablet (NDC 69367-0677-01)
Lists sugar (sucrose or dextrose)
- Atlantic Biologicals: 0.125 mg/5 mL oral solution (NDC 17856-0511-02), 0.125 mg/5 mL oral solution (NDC 17856-0514-05)
- Chartwell RX: 0.125 mg/5 mL oral solution, 0.125 mg/mL oral solution
- Lannett: 0.125 mg/5 mL oral solution, 0.125 mg/mL oral solution
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 Hyoscyamine inactive ingredients
Is Hyoscyamine gluten-free?
Does Hyoscyamine contain lactose?
Does Hyoscyamine contain soy?
Is there a dye-free Hyoscyamine?
Does Hyoscyamine 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 Hyoscyamine 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 Hyoscyamine guide