Gluten Screen

Last verified May 17, 2026 · 11 product labels screened

Is cephalexin gluten-free?

Looks mostly clean — worth verifying with the maker. Mostly yes — but worth a quick call to the manufacturer for some generics. Of 11 product labels we checked, 10 are clean, 0 are confirmed gluten-free by the maker, and 1 contain an inactive ingredient (typically a source-ambiguous starch) whose botanical origin isn't fully disclosed. None contained confirmed gluten.

Drug context

About cephalexin

Cephalexin is a first-generation cephalosporin antibiotic for skin and respiratory infections, sold under brand names including Keflex.

Why this matters

Different manufacturers, different ingredients

Generics of cephalexin use the same active ingredient, but they aren't required to use the same inactive ingredients. Your pharmacy may switch which manufacturer they dispense between fills, sometimes without telling you. The list below shows each manufacturer's product label as a separate entry, because that's the granularity that actually matters when you're celiac.

The labels

The 11 we checked

  1. 01
    Aurobindo worth a call to confirm

    Plogsted list · Cephalexin (Aurobindo, Lupin, Novopharm, Teva) · label dated 2017-04-28

    View source label →
  2. 02
    AX Pharmaceutical Corp nothing flagged on the label

    US label (DailyMed) · CEPHALEXIN MONOHYDRATE POWDER [AX PHARMACEUTICAL CORP] · label dated May 06, 2026

    View source label →
  3. 03
    Coupler LLC nothing flagged on the label

    US label (DailyMed) · CEPHALEXIN CAPSULE [COUPLER LLC] · label dated Apr 30, 2026

    Inactive ingredients CELLULOSE, MICROCRYSTALLINE · D&C YELLOW NO. 10 · FD&C BLUE NO. 1 · FD&C GREEN NO. 3 · FD&C YELLOW NO. 6 · FERROSOFERRIC OXIDE · GELATIN · MAGNESIUM STEARATE · POTASSIUM HYDROXIDE · PROPYLENE GLYCOL · SHELLAC · TITANIUM DIOXIDE

    View source label →
  4. 04
    Lupin Pharmaceuticals, Inc. nothing flagged on the label

    US label (DailyMed) · CEPHALEXIN FOR SUSPENSION [LUPIN PHARMACEUTICALS, INC.] · label dated Apr 02, 2026

    Inactive ingredients FD&C RED NO. 40 · SILICON DIOXIDE · SODIUM BENZOATE · STRAWBERRY · SUCROSE · XANTHAN GUM

    View source label →
  5. 05
    Direct_Rx nothing flagged on the label

    US label (DailyMed) · CEPHALEXIN CAPSULE [DIRECT_RX] · label dated Mar 30, 2026

    Inactive ingredients AMMONIA · ANHYDROUS LACTOSE · D&C YELLOW NO. 10 · FD&C BLUE NO. 1 · FERROSOFERRIC OXIDE · GELATIN · MAGNESIUM STEARATE · POTASSIUM HYDROXIDE · PROPYLENE GLYCOL · SHELLAC · SILICON DIOXIDE · SODIUM LAURYL SULFATE · TITANIUM DIOXIDE

    View source label →
  6. 06
    Sportpharm LLC nothing flagged on the label

    US label (DailyMed) · CEPHALEXIN CAPSULE [SPORTPHARM LLC] · label dated Mar 26, 2026

    Inactive ingredients AMMONIA · ANHYDROUS LACTOSE · D&C YELLOW NO. 10 · FD&C BLUE NO. 1 · FERROSOFERRIC OXIDE · GELATIN · MAGNESIUM STEARATE · POTASSIUM HYDROXIDE · PROPYLENE GLYCOL · SHELLAC · SILICON DIOXIDE · SODIUM LAURYL SULFATE · TITANIUM DIOXIDE

    View source label →
  7. 07
    Preferred Pharmaceuticlas Inc. nothing flagged on the label

    US label (DailyMed) · CEPHALEXIN FOR SUSPENSION [PREFERRED PHARMACEUTICLAS INC.] · label dated Mar 26, 2026

    Inactive ingredients FD&C RED NO. 40 · METHYLCELLULOSE (15 MPA.S) · METHYLCELLULOSE (400 MPA.S) · SILICON DIOXIDE · SODIUM BENZOATE · STRAWBERRY · SUCROSE · XANTHAN GUM

    View source label →
  8. 08
    Direct_Rx nothing flagged on the label

    US label (DailyMed) · CEPHALEXIN CAPSULE [DIRECT_RX] · label dated Mar 18, 2026

    Inactive ingredients AMMONIA · ANHYDROUS LACTOSE · D&C YELLOW NO. 10 · FD&C BLUE NO. 1 · FERROSOFERRIC OXIDE · GELATIN · MAGNESIUM STEARATE · POTASSIUM HYDROXIDE · PROPYLENE GLYCOL · SHELLAC · SILICON DIOXIDE · SODIUM LAURYL SULFATE · TITANIUM DIOXIDE

    View source label →
  9. 09
    Sportpharm LLC nothing flagged on the label

    US label (DailyMed) · CEPHALEXIN CAPSULE [SPORTPHARM LLC] · label dated Feb 05, 2026

    Inactive ingredients CELLULOSE, MICROCRYSTALLINE · D&C YELLOW NO. 10 · FD&C BLUE NO. 1 · FD&C GREEN NO. 3 · FD&C YELLOW NO. 6 · FERROSOFERRIC OXIDE · GELATIN · MAGNESIUM STEARATE · POTASSIUM HYDROXIDE · PROPYLENE GLYCOL · SHELLAC · TITANIUM DIOXIDE

    View source label →
  10. 10
    Sportpharm LLC nothing flagged on the label

    US label (DailyMed) · CEPHALEXIN CAPSULE [SPORTPHARM LLC] · label dated Feb 05, 2026

    Inactive ingredients AMMONIA · ANHYDROUS LACTOSE · D&C YELLOW NO. 10 · FD&C BLUE NO. 1 · FD&C RED NO. 40 · FERROSOFERRIC OXIDE · GELATIN · MAGNESIUM STEARATE · POTASSIUM HYDROXIDE · PROPYLENE GLYCOL · SHELLAC · SILICON DIOXIDE · SODIUM LAURYL SULFATE · TITANIUM DIOXIDE

    View source label →
  11. 11
    Northwind Health Company, LLC nothing flagged on the label

    US label (DailyMed) · CEPHALEXIN CAPSULE [NORTHWIND HEALTH COMPANY, LLC] · label dated Jan 12, 2026

    Inactive ingredients CROSCARMELLOSE SODIUM · D&C YELLOW NO. 10 · FD&C BLUE NO. 1 · FD&C YELLOW NO. 6 · GELATIN, UNSPECIFIED · MAGNESIUM STEARATE · MICROCRYSTALLINE CELLULOSE · SODIUM LAURYL SULFATE · TITANIUM DIOXIDE

    View source label →

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Background

What “gluten in a medication” actually means

Gluten enters drugs through their excipients — the inactive ingredients used to bind, coat, fill, or stabilize the dose. The main concern is wheat starch as a filler. Source-ambiguous starches (plain “starch”, pregelatinized starch, sodium starch glycolate, modified starch) get flagged for verification because their botanical origin isn't always disclosed on the label.

The 2024 Mangione et al. pediatric NDC analysis (689 NDCs across the top 100 pediatric medications) found 1.5% contained gluten outright; another 25.7% couldn't be confirmed either way. Liquid and oral-suspension formulations carry disproportionate risk because wheat starch is a common thickener. Full methodology →

Keep checking

Other drugs people look up

Important. This page is informational. Drug labels can change without notice; a manufacturer attestation is point-in-time, not a warranty. If you have celiac disease and your pharmacy switches manufacturers, re-screen the new label before taking the dispensed product. For a definitive answer, call the manufacturer's medical-information line with the NDC code from your prescription bottle.