Glycopyrronium Topical
Glycopyrronium topical is an anticholinergic medicine used to treat primary axillary hyperhidrosis (excessive underarm sweating) in adults and children aged 9 and older.
🧬 Where this information comes from Click to expand
The clinical label records used on this page are FDA-filed Structured Product Labeling (SPL) retrieved through openFDA. We identified 1 clinical label set within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. Forms, routes, brands, labelers, strengths, and NDC product-record counts are built separately from matching FDA National Drug Code Directory records. The linked DailyMed document is a representative official source for verification, not the page’s only clinical source. View the linked label on DailyMed →
📖 Glycopyrronium Topical: Patient Information Guide
A plain-language walkthrough of Glycopyrronium Topical — what it treats, how it works, how it’s taken, side effects, warnings and interactions. Tap any section to expand it.
🎯What it's used for▾
Glycopyrronium topical is approved for one specific condition:
- Qbrexza (topical cloth): treatment of primary axillary hyperhidrosis (excessive underarm sweating with no underlying medical cause) in adults and in children and adolescents aged 9 years and older.
⚙️How it works▾
Glycopyrronium is an anticholinergic — it works by blocking acetylcholine receptors on sweat glands in the underarm. Acetylcholine is the chemical messenger your nervous system uses to tell those glands to produce sweat. When glycopyrronium blocks that receptor, the signal doesn't get through, and sweat production is reduced. Because it's applied directly to the skin, the effect is largely local rather than system-wide.
💊How it's taken▾
Qbrexza is applied topically to both underarms once daily using a single pre-moistened cloth. Apply it to clean, dry, unbroken skin. One cloth covers both underarms — wipe each side once. Do not apply it to other areas of the body, and do not use it more than once every 24 hours. Always wash your hands immediately after applying and discarding the cloth. Follow your prescriber's instructions for your specific situation.
🤒Side effects — in detail▾
The most common side effects reported in clinical trials include:
- Dry mouth (the most frequently reported, affecting roughly 1 in 4 users in trials)
- Dilated pupils (mydriasis) and blurred vision
- Difficulty starting to urinate (urinary hesitation)
- Headache
- Dry eyes, nasal dryness, and dry throat
- Constipation
- Dry skin
- Local skin reactions: redness (erythema), burning or stinging, and itching at the underarm application site
If you develop trouble urinating, stop sweating entirely in the heat, or experience blurred vision that does not go away, stop using Qbrexza and contact your doctor promptly.
⚠️Warnings & precautions▾
- Urinary retention: Qbrexza can cause new or worsening difficulty passing urine, even in people with no prior history of urinary problems. Stop use immediately and call your doctor if you notice trouble urinating or a distended, uncomfortable bladder.
- Heat illness risk: Because this medicine reduces sweating, your body may struggle to cool down in hot or very warm conditions. Watch for a complete absence of sweating in the heat, which can lead to hyperpyrexia (dangerous overheating) or heat stroke. Avoid use if this happens.
- Blurred vision: Transient (temporary) blurred vision can occur. Do not drive, operate heavy machinery, or do hazardous work if your vision is affected. Stop use until vision clears.
- Accidental exposure — especially in children: Used cloths discarded in the trash have caused accidental eye exposure in children, leading to dilated pupils and blurred vision. Always wash hands after use and keep discarded cloths out of reach of children.
🔀What it interacts with▾
Qbrexza has one key interaction category to know about:
- Other anticholinergic medications: Taking Qbrexza alongside other drugs that have anticholinergic effects (such as certain medications for overactive bladder, some antihistamines, or some antidepressants) can add up the anticholinergic side effects — making dry mouth, urinary problems, blurred vision, and constipation more likely or more severe. Avoid combining them unless your doctor has reviewed your full medication list.
This is not a complete list of interactions. Always talk with your doctor or pharmacist before starting, stopping, or changing any medication.
📋Before taking it▾
- Do not use Qbrexza if you have glaucoma, myasthenia gravis (a nerve-muscle condition causing muscle weakness), a blocked bowel (paralytic ileus), severe ulcerative colitis or toxic megacolon, unstable cardiovascular status during acute bleeding, or Sjogren's syndrome.
- Tell your doctor if you have an enlarged prostate, bladder-neck obstruction, or any history of urinary retention — Qbrexza may worsen these conditions.
- Use with extra caution in hot weather or during exercise; reduced sweating raises the risk of overheating.
- Children under 9 years of age: safety and effectiveness have not been established.
- Older adults (65+): there is limited clinical trial data in this age group; use with care.
- Kidney disease: the body clears glycopyrronium much more slowly in people with kidney failure; tell your doctor if you have kidney problems.
- Pregnancy: there are no adequate human data on safety during pregnancy. Talk to your doctor before using Qbrexza if you are pregnant or planning to become pregnant.
- Breastfeeding: it is unknown whether glycopyrronium passes into breast milk. Discuss the benefits and risks with your doctor.
🚑If you take too much▾
Using too much Qbrexza on the skin could increase local skin irritation and raise the risk of anticholinergic side effects such as dry mouth, urinary retention, flushing, rapid heartbeat, overheating, and dilated pupils. Applying it under tight or bandage-style dressings (occlusive conditions) may also cause increased absorption and stronger effects. If a severe or life-threatening reaction is suspected, seek emergency medical care immediately — treatment may include managing the individual symptoms and, in serious cases, a reversal agent called neostigmine.
🔬Pharmacokinetics — how your body processes it▾
After applying Qbrexza once daily to the underarms, glycopyrronium is absorbed through the skin and detectable in the bloodstream within about 1 to 1.5 hours on average, with no significant buildup over repeated daily use. Most of the drug is eliminated unchanged through the urine; only a small fraction is metabolized. In people with kidney failure, the body's ability to clear glycopyrronium is significantly reduced, which could increase exposure. The pharmacokinetics of Qbrexza have not been formally studied in people with liver problems or in pregnant women.
📦How to store it▾
Store at room temperature 20° - 25°C (68° - 77°F); excursions permitted to 15° - 30°C (59° - 86°F) . keep away from heat or flame.
📄 Written from Glycopyrronium Topical’s FDA-approved label information, summarized in plain language with AI, and reviewed by our pharmacy team before publication. Every point is grounded in that labeling — nothing is invented. How we use AI →
Supplements & herbs that interact with Glycopyrronium Topical
49 supplements and herbal products have documented interactions with Glycopyrronium Topical in the licensed clinical database we use. Most are manageable — but your pharmacist should know about everything you take, including vitamins and herbals.
- Major · 3
- Moderate · 34
- Minor · 12
Educational information from a licensed clinical database (Natural Medicines) — see our data sources & update cadence. Not medical advice: an interaction being documented does not mean it will happen to you; do not start or stop medications or supplements without professional guidance.
🩺 Pharmacist Counseling Corner
Quick, plain-English answers to the questions patients ask most about Glycopyrronium Topical — the kind of thing our pharmacy team would talk through with you at the counter.
What exactly is Qbrexza and what is it supposed to do? ▾
How do I use it correctly? ▾
What side effects should I expect, and which ones should I call the doctor about? ▾
I live in a hot climate. Is there anything extra I need to watch for? ▾
Can I use this if I'm pregnant or breastfeeding? ▾
Are there any medicines I should avoid while using Qbrexza? ▾
Is Glycopyrronium Topical available over the counter? ▾
When was Glycopyrronium Topical first available? ▾
💬 Answers drafted from Glycopyrronium Topical’s FDA-approved label information, summarized in plain language with AI, and reviewed by our pharmacy team before publication. Grounded in that labeling — nothing is made up. How we use AI →
🧰 Keep exploring
💊 How Glycopyrronium Topical comes
Glycopyrronium Topical is available in 1 form. Different forms and brands can have different approved uses, doses, schedules, and directions. Follow the instructions for your exact product, and do not switch forms without guidance from your prescriber or pharmacist.
Topical cream, ointment or gel
How this form is used
- Qbrexza is used to treat primary axillary hyperhidrosis (excessive underarm sweating) in adults and children aged 9 and older.
- Qbrexza comes as a single-use pre-moistened cloth; open the pouch, unfold the cloth, and wipe it across one underarm, then use the same cloth on the other underarm.
- Qbrexza should be applied once daily to clean, dry, unbroken underarm skin only — do not use it on other parts of the body.
- Wash your hands with soap and water immediately after applying and discarding the Qbrexza cloth to avoid accidental eye exposure.
- Do not apply Qbrexza under tight or occlusive dressings, and do not use it more than once every 24 hours.
📊 Glycopyrronium Topical across the U.S. market
How Glycopyrronium Topical appears in the FDA’s National Drug Code Directory — including its dosage forms, strengths, brand names, manufacturers, and FDA-listed product records. These are directory records, not sales or prescription volume.
🔍 Compare Glycopyrronium Topical products
A representative set of FDA-listed product records for Glycopyrronium Topical — across manufacturers, strengths, and dosage forms, grouped by form with each product’s manufacturer and how the FDA approved it. The same medicine may be made and packaged by different companies, so a single drug can have many directory entries. (It’s also why a refill can look different — a new shape, color, or box — even though it contains the same medication.)
| Strength | Route | Manufacturer / Labeler | Category ⓘ | Details |
|---|---|---|---|---|
| 💊Topical cream, ointment or gel | ||||
| 2.4 g/100 g | Topical | Journey Medical Corporation × 4 listings | NDA | View NDC → |
Showing 4 of 4 products — FDA National Drug Code Directory. See every product, package size and price: browse all 4 Glycopyrronium Topical NDCs →
📈 What people report — real-world data (FDA FAERS)
After a medicine reaches the market, patients, doctors and drugmakers can send the FDA reports of problems they think may be linked to it. Here’s what’s been reported for Glycopyrronium Topical — a signal of what to watch for, not proof the drug caused it.
Source: openFDA, from the FDA Adverse Event Reporting System (FAERS). These are voluntary reports — they don’t prove the drug caused the effect, and counts reflect how often something was reported, not how often it actually happens. Reports also often name the very problem the medicine is taken for — a common reason to file one is that the drug didn’t help — so for a pain reliever you may see “pain” high on the list; that points to why the report was filed, not to the drug causing the symptom. This counts every report that lists Glycopyrronium Topical in any role, so the total runs higher than the FDA’s official dashboard, which counts only cases where the drug is the suspect. For the authoritative figures, see the FDA FAERS Public Dashboard. Always talk to your pharmacist or doctor.
🏛️ The road to your pharmacy
How Glycopyrronium Topical went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
🚨 Recall history
A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.
Source: openFDA drug enforcement (recall) reports.
RxNorm Concept Web — From Ingredient to Every Form and Strength
This page starts with one ingredient concept (IN). The branches below show its dose-form concepts (SCDF), then the available clinical drug and strength concepts (SCD). Combination products remain separate concepts with their own pages.
RxCUI 1546438 8 dose forms · 14 strengths
-
Dose form (SCDF) Disintegrating Oral Tablet RxCUI 2589273No current FDA listingClinical drug / strength (SCD) glycopyrrolate 1.7 MGRxCUI 2589274 -
Dose form (SCDF) Inhalation Solution RxCUI 2108425No current FDA listingClinical drug / strength (SCD) glycopyrrolate 0.025 MG/MLRxCUI 1992566 -
Dose form (SCDF) Injectable Solution RxCUI 372339No current FDA listingClinical drug / strength (SCD) glycopyrrolate 0.2 MG/MLRxCUI 238212 -
Dose form (SCDF) Injection RxCUI 1731581No current FDA listingClinical drug / strength (SCD) 1 ML glycopyrrolate 0.2 MG/MLRxCUI 17315822 ML glycopyrrolate 0.2 MG/MLRxCUI 1731590 -
Dose form (SCDF) Medicated Pad RxCUI 2054109No current FDA listingClinical drug / strength (SCD) 24 MG/MLRxCUI 2054118 -
Dose form (SCDF) Oral Solution RxCUI 999960No current FDA listingClinical drug / strength (SCD) glycopyrrolate 0.2 MG/MLRxCUI 999961 -
Dose form (SCDF) Oral Tablet RxCUI 372340No current FDA listingClinical drug / strength (SCD) glycopyrrolate 1 MGRxCUI 197738glycopyrrolate 1.5 MGRxCUI 1247658glycopyrrolate 2 MGRxCUI 197739 -
Dose form (SCDF) Prefilled Syringe RxCUI 2101489No current FDA listingClinical drug / strength (SCD) 1 ML glycopyrrolate 0.2 MG/MLRxCUI 21014902 ML glycopyrrolate 0.2 MG/MLRxCUI 21014953 ML glycopyrrolate 0.2 MG/MLRxCUI 24733835 ML glycopyrrolate 0.2 MG/MLRxCUI 2371710
Look up RxCUI 1546438 in the RxCUI Atlas →
RxNorm is the U.S. National Library of Medicine’s normalized drug vocabulary. Its concept hierarchy can include forms that are not currently marketed; the status on each branch compares that concept with current FDA listings. RxCUIs identify vocabulary concepts, not individual packages or manufacturers.
📦 Supply & shortage status
Whether Glycopyrronium Topical is in short supply in the U.S. right now, plus any shortage history the FDA has on record. A shortage usually reflects a manufacturing or demand issue — not a safety problem with the drug.
Source: openFDA, from the FDA Drug Shortages database.
🏷️ Sold under these brand names
🏭 Manufacturers & labelers
RxNorm drug class
Glycopyrronium Topical belongs to the Anticholinergic class.
Classified by RxNorm RxClass — the U.S. National Library of Medicine's standardized drug-classification service (Established Pharmacologic Class from the FDA, the ATC drug family from the WHO, and mechanism of action). Reference only, not medical advice.
🔬 Where this comes from
Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.
How we combine label and product data
HelloPharmacist combines public FDA and NLM records; we don’t author the underlying clinical facts. We identified 1 FDA-filed SPL label set within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. The representative label is the starting point for the displayed reference monograph; the 12 largest stored in-scope SPL records, which may include that representative, are compared section by section, and the longest available version of each section is retained. Forms, routes, brands, labelers, product-listed strengths, and product-record counts are aggregated separately from ingredient-matched FDA NDC Directory records; package records listed above are associated with the linked SPL; and the normalized concept hierarchy comes from NLM RxNorm.
Where a section is identified as AI-written, its plain-language text is generated from bounded label evidence. New draft drug pages remain in the admin review queue before first publication. Journey Medical Corporation is the representative DailyMed label linked for verification and dates; it is not the sole source used for the page.
This is general education, not medical advice — always consult your doctor or pharmacist about your medications and any medical condition. For the exact wording of the linked representative label, view that label on DailyMed; some displayed composite sections may come from other in-scope SPL labels. Learn how we use AI and our data sources & update cadence.