Bactoshield CHG CHLORHEXIDINE GLUCONATE 40 mg/mL Liquid, 473 mL
by SC Johnson Professional USA, Inc. · 473 mL in 1 BOTTLE (11084-128-34)
NDC 11084-0128-34
🏷️ FDA NDC (as labeled)
11084-128-34
billing pads the product segment with a zero
This package
Contains473 mL
Pack sizes4 compare ↓
OTC
Brand
Discontinued
Non-controlled
⚠ Discontinued by firm
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
⚠️
Excluded from the active FDA NDC Directory.
The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory.
Search the FDA NDC Directory ↗
🆔 Identity & classification
FDA NDC (as labeled)
11084-128-34
Product NDC
11084-128
11-digit billing NDC
11084012834
UNII
MOR84MUD8E
Application #
NDA019258
SPL Set ID
5d49522f-63e5-4297-adf5-b5f3bd419d47
Physiologic effect
Decreased Cell Wall Integrity
DEA schedule
Non-controlled
Marketing category
NDA
Marketing status
Discontinued
FDA listing status
Discontinued by firm
Marketing start
2019-08-15
Route
TOPICAL
Dosage form
LIQUID
Substance
CHLORHEXIDINE GLUCONATE
Why two NDCs?
The FDA registers this code as 11084-128-34 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 11084-0128-34. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.
🏷️ RxNorm drug class
This medicine belongs to the Antiinfectives and antiseptics for local oral treatment class.
Drug family (ATC)
Antiinfectives and antiseptics for local oral treatment, Antiinfectives, Biguanides and amidines
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.
🏭 Manufacturer & labeler
LabelerSC Johnson Professional USA, Inc.
Application holderECOLAB INC
FDA applicationNDA019258 (NDA)
Labeler code11084
First marketedAug 2019
Product typeHuman Otc Drug
Portfolio16 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.
🩺 Clinical
📗 Our plain-language guide HelloPharmacist
- It's actually a prescription-strength antimicrobial rinse, which is different from over-the-counter mouthwash. Your dentist prescribes it specifically to treat gingivitis — that's...
- What exactly is chlorhexidine rinse for — is it just like a regular mouthwash?
- Yes, tooth and surface staining is one of the most common side effects of chlorhexidine oral rinse. It can also increase tartar buildup on your teeth. The good news is that this is...
- My teeth look like they're staining — is that from the rinse?
Patient education
Supplement & herbal interactions
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.
💬 Questions about CHLORHEXIDINE GLUCONATE?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 Inactive Ingredients / Excipients
Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
-
UNII QWA2IZI6FI
A surfactant derived from coconut oil, cocamine oxide helps reduce surface tension and improves how ingredients mix together in liquid formulations, enhancing product stability and texture.
-
UNII 92005F972D
A foaming and thickening agent derived from coconut oil. It's used in liquid medicines to improve texture, help distribute active ingredients evenly, and create a pleasant consistency for easier swallowing or application.
-
UNII R4R8J0Q44B
Gluconic acid is an organic acid derived from glucose. It functions as a buffer and pH adjuster in medicines, helping maintain the product's acidity or alkalinity for stability and proper absorption.
-
UNII WQ29KQ9POT
Gluconolactone is a mild organic acid derived from glucose. It functions as a buffer and pH regulator in medicines, helping maintain stable acidity levels and improve product stability.
-
UNII X70SE62ZAR
Hydroxyethyl cellulose is a plant-derived thickener made from cellulose. It's used in medicines as a binder to hold ingredients together, a thickener for gels or liquids, and sometimes as a coating agent.
-
UNII ND2M416302
Isopropyl alcohol is a clear liquid solvent derived from petroleum. In medicines, it dissolves active ingredients and other components, helps the product flow smoothly, and aids in sterilization during manufacturing.
-
UNII 6F36Q0I0AC
PEG-150 distearate is a waxy substance made by combining polyethylene glycol with stearic acid. It acts as an emulsifier and surfactant to help blend water and oil-based ingredients, and may also function as a thickener or lubricant in the formulation.
-
UNII 09179OX7TB
PEG-75 Lanolin is a waxy substance derived from sheep's wool that has been chemically modified to mix easily with water and oil. It acts as an emulsifier and moisturizer in topical formulations, helping blend different ingredients and soften the skin.
-
UNII 6DC9Q167V3
Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
-
UNII XPS4174QZJ
A synthetic compound used as an antimicrobial preservative in topical medicines and personal care products. It helps prevent bacterial and fungal growth, extending the product's shelf life.
-
UNII 059QF0KO0R
Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
11 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statescocamide DEA, cocamine oxide, fragrance, gluconic acid contains one or more of these ingredients, gluconolactone, hydroxyethyl cellulose, isopropyl alcohol 4%, PEG-75 lanolin, PEG-150 distearate, propylene glycol, quaternium-60, water
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed —
ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.
💲 Pricing
A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.
| Price system | Per mL | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | Not in the retail survey — common for institutional, discontinued, or low-volume packs. | |
| Medicaid paysCMS SDUD · 12 mo | No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data. | |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
ℹ️
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Antiseptic Skin Cleanser 4 g/100mL 70000-0407-01 | Cardinal | 237 ml | $0.025 | — | FDA listed | — |
| Antiseptic Skin Cleanser 4 g/100mL 00116-1061-04 | Xttrium | 118 ml | $0.034 | — | Availability likely | — |
| Antiseptic Skin Cleanser 4 mg/100mL 46122-0137-34 | AmerisourceBergen | 237 ml | $0.037 | — | Availability likely | — |
| Foster and Thrive 4 g/100mL 70677-1221-01 | McKesson | 237 ml | $0.037 | — | Availability likely | — |
| Chlorhexidine Gluconate 40 mg/mL 16571-0111-12 | Rising | 118 ml | $0.041 | — | Availability likely | — |
| Betasept .04 mg/mL 67618-0200-04 | Atlantis | 118 ml | $0.041 | — | Availability likely | — |
| Cardinal Health 4 g/100mL 00116-0061-04 | Xttrium | 118 ml | — | — | Discontinued | — |
| Antiseptic Skin Cleanser 4 mg/100mL 00116-0137-34 | Xttrium | 237 ml | — | — | FDA listed | — |
| Antiseptic Skin Cleanser 4 mg/100mL 00116-0161-08 | Xttrium | 237 ml | — | — | FDA listed | — |
| Betasept .04 mg/mL 00116-0200-01 | Xttrium | 3785 ml | — | — | FDA listed | — |
| Antiseptic Skin Cleanser 4 mg/100mL 00116-0401-50 | Xttrium | 237 ml | — | — | FDA listed | — |
| Antiseptic Skin Cleanser 4 g/100mL 00116-0407-01 | Xttrium | 237 ml | — | — | FDA listed | — |
| Antiseptic Skin Cleanser 4 g/100mL 00116-0767-08 | Xttrium | 237 ml | — | — | FDA listed | — |
| CliniClean 4 g/100mL 00116-0901-05 | Xttrium | 118 ml | — | — | Discontinued | — |
| Dyna-Hex 4 4 g/100mL 00116-1060-18 | Xttrium | 535 ml | — | — | FDA listed | — |
| Foster and Thrive 4 g/100mL 00116-1221-01 | Xttrium | 237 ml | — | — | FDA listed | — |
| Bactoshield CHG 40 mg/mL 00116-1344-08 | Xttrium | 3780 ml | — | — | FDA listed | — |
| Antiseptic Skin Cleanser 4 mg/100mL 00116-3678-07 | Xttrium | 473 ml | — | — | FDA listed | — |
| Hibiclens 4 g/100mL 00234-0575-40 | Molnlycke | 118 ml | — | — | FDA listed | — |
| Antiseptic Skin Cleanser 4 mg/100mL 00363-1061-08 | Walgreen | 237 ml | — | — | FDA listed | — |
| Maxiclens Chlorhexidine Gluconate Liquid Solution, 4% 40 mg/mL 00404-0219-01 | Henry | 118 ml | — | — | FDA listed | — |
| Maxiclens Chlorhexidine Gluconate Liquid Solution, 4% 40 mg/mL 00404-0220-03 | Henry | 236 ml | — | — | FDA listed | — |
| Maxiclens Chlorhexidine Gluconate Liquid Solution, 4% 40 mg/mL 00404-0221-04 | Henry | 473 ml | — | — | FDA listed | — |
| Bactoshield CHG 40 mg/mL 11084-0039-03 | SC | 118 ml | — | — | FDA listed | — |
| Bactoshield CHG 40 mg/mLthis 11084-0128-34 | SC | 473 ml | — | — | Discontinued | — |
| Antiseptic Skin Cleanser 4 g/100mL 11822-0116-05 | Rite | 237 ml | — | — | FDA listed | — |
| Antiseptic Skin Cleanser 4 g/100mL 11822-0891-02 | Rite | 532 ml | — | — | FDA listed | — |
| Antiseptic Skin Cleanser 4 mg/100mL 11822-3678-07 | Rite | 473 ml | — | — | FDA listed | — |
| BD E-Z Scrub 107 40 g/1000mL 17271-0107-03 | Becton | 18 ml | — | — | FDA listed | — |
| Antiseptic Skin Cleanser 4 mg/100mL 36800-0401-50 | Topco | 237 ml | — | — | FDA listed | — |
| Halyard Chlorhexidine Gluconate 40 mg/mL 39892-0960-01 | Owens | 118 ml | — | — | FDA listed | — |
| Halyard Chlorhexidine Gluconate 40 mg/mL 39892-0961-01 | Owens | 118 ml | — | — | FDA listed | — |
| Antiseptic Skin Cleanser 4 mg/100mL 41250-0162-08 | Meijer | 237 ml | — | — | Discontinued | — |
| Scrub, Scrub-Stat, Foam Safe, Micro-Guard 40 mg/mL 42939-0125-19 | AVA, | 946 ml | — | — | FDA listed | — |
| Scrub, Scrub-Stat, Foam Safe, Micro-Guard 40 mg/mL 42939-0128-01 | AVA, | 118 ml | — | — | FDA listed | — |
| Scrub-Stat 40 mg/mL 47593-0464-11 | Ecolab | 3780 ml | — | — | FDA listed | — |
| Scrub-Stat 40 mg/mL 47593-0468-21 | Ecolab | 208000 ml | — | — | Discontinued | — |
| Antiseptic Skin Cleanser 4 g/100mL 59779-0767-08 | CVS | 237 ml | — | — | FDA listed | — |
| Antiseptic Skin Cleanser 4 mg/100mL 63868-0940-08 | Chain | 237 ml | — | — | FDA listed | — |
| Antiseptic Skin Cleanser 4 g/100mL 68599-5401-00 | McKesson | 4 bottles | — | — | FDA listed | — |
| CliniClean 4 g/100mL 69464-0901-05 | HR | 118 ml | — | — | Discontinued | — |
| Hibiclens 4 g/100mL 76420-0535-08 | Asclemed | 236 ml | — | — | FDA listed | — |
| Surgical Scrub Brush/Sponge With Nail Cleaner 4% CHG 4 g/100mL 84128-0003-01 | Xinxiang | 30 patches | — | — | FDA listed | — |
About this product: this is the brand-name version. Some generic versions are approved by the FDA, but we could not confirm current pharmacy availability from our pricing/market data.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.
⏳ Availability & generic status
🏛️
2019
On the market since
Aug 2019
📍
2026
Currently FDA-listed
7 years listed
🔒
·
Generic approved (availability unconfirmed)
see note
🔒Generic approved by FDA, but pharmacy availability is not confirmed
The FDA lists approved generic versions of this medicine, but that does not always mean a pharmacy can get one today. Patent rules, launch agreements, supply and pricing can affect when generics actually arrive.
Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.
📊 Medicare Part D spend CMS · PART D · 2026 (Q1)
Medicare Part D (outpatient prescription) spending for Chlorhexidine Gluconate (matched by generic name) — the program that covers self-administered drugs. 7 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Chlorhexidine Gluconate. CMS lists 2 products for this generic; we show the highest-spend one. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$3.96M
Claims incl. refills
658.9K
Beneficiaries
540.1K
Spend / beneficiary
$7.34
Spend / claim
$6.02
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 11084-0128-03 | 118 mL in 1 BOTTLE (11084-128-03) | 2019-08-15 | Active |
| 11084-0128-08 | 3785 mL in 1 BOTTLE (11084-128-08) | 2019-08-15 | Discontinued by firm |
| 11084-0128-24 | 946 mL in 1 BOTTLE (11084-128-24) | 2019-08-15 | Active |
| 11084-0128-34 You're viewing this | 473 mL in 1 BOTTLE (11084-128-34) | 2019-08-15 | Discontinued by firm |
You're viewing one of 4 pack sizes for this product.
Pack size FAQ
What quantity is in NDC 11084-0128-34?
NDC 11084-0128-34 contains 473 mL — 473 ml in 1 bottle.
What is the difference between NDC 11084-0128-34 and NDC 11084-0128-03?
Both are Bactoshield CHG CHLORHEXIDINE GLUCONATE 40 mg/mL Liquid — the drug itself is identical. NDC 11084-0128-34 is the 473 mL package, while NDC 11084-0128-03 is the 118 ml package.
What NDC number is used to bill for this package of Bactoshield CHG CHLORHEXIDINE GLUCONATE 40 mg/mL Liquid?
Bill NDC 11084-0128-34 — the 11-digit billing format is 11084012834. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.
🧭 About this NDC listing & data coverage
Over-the-counter (OTC) product
No longer marketed (per FDA listing data)
What data is (and isn’t) available for this NDC — tap to expand
| NDC identity (package / product / labeler codes) | ✓ Available |
| Labeler | ✓ Available |
| Product & package description | ✓ Available |
| Marketing category & status | ✓ Available |
| Active ingredient / dosage form / route | ✓ Available |
| FDA label (SPL via DailyMed) | ✓ Available |
| Package photos | ✓ Available |
| Inactive ingredients (structured) | ✓ Available |
| NADAC pharmacy acquisition price (CMS) | — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey. |
| Orange Book / therapeutic-equivalence data | — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope. |
| HCPCS J-code billing crosswalk | — Not published for this NDC Most self-administered / retail products have no J-code — that is normal. |
| Medicaid utilization (CMS SDUD) | — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold. |
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.
Questions about this listing
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 11084-128-34, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 11084-0128-34, written without dashes as 11084012834. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 11084-0128-34, the first segment (11084) is the labeler code FDA assigned to SC Johnson Professional USA, Inc.; the middle segment (0128) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (34) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 3 other package presentations of this same product, including 118 ml (11084-0128-03), 946 ml (11084-0128-24), 3785 ml (11084-0128-08). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
SC Johnson Professional USA, Inc. is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
📄 FDA label — Drug Facts FDA SPL
The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage
⏱️ Dosage and Administration
⚠️ Warnings
📦 Storage and Handling
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
🎯 Indications and Usage ▾
Uses surgical hand scrub: significantly reduces the number of microorganisms on the hands and forearms prior to surgery or patient care healthcare personnel handwash: handwash to help reduce bacteria that potentially can cause disease skin wound and general skin cleanser: helps reduce bacteria on the skin
⏱️ Dosage and Administration ▾
Directions use with care in premature infants or infants under 2 months of age. These products may cause irritation or chemical burns. use full strength do not dilute Surgical hand scrub remove jewelry wet hands and forearms with water and apply 5 mL of the product wash/scrub hands and forearms for 3 minutes paying particular attention to the nails, cuticles, and interdigital spaces rinse thoroughly with water wash for an additional 3 minutes with 5 mL of the product and rinse under running water dry thoroughly Healthcare personnel handwash wet hands with water dispense about 5 mL of product into cupped hands and wash in a vigorous manner for 30 seconds rinse and dry thoroughly Skin wound and general skin cleanser thoroughly rinse the area to be cleansed with water apply the minimum amount of product necessary to cover the skin or wound area and wash gently.
Rinse thoroughly with water. rinse again thoroughly
⚠️ Warnings ▾
Warnings For external use only Allergy alert This product may cause a severe allergic reaction. Symptoms may include: wheezing/difficulty breathing shock facial swelling hives rash If an allergic reaction occurs, stop use and seek medical help right away. Do not use if you are allergic to chlorhexidine gluconate or any other ingredient in this preparation as a patient preoperative skin preparation (especially on the head or face) in contact with meninges in the genital area When using this product keep out of eyes, ears, and mouth.
May cause serious and permanent eye injury if placed or kept in the eye during surgical procedures or may cause deafness when instilled in the middle ear through perforated eardrums. if contact occurs, rinse with cold water right away wounds which involve more than the superficial layers of the skin should not be routinely treated repeated general skin cleansing of large body areas should not be done except when an underlying condition makes it necessary to reduce the bacterial population of the skin Stop use and ask a doctor if irritation, sensitization or allergic reaction occurs and lasts for 72 hours.
These may be signs of a serious condition. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
📦 Storage and Handling ▾
Other information store between 20-25°C (68-77°F) avoid excessive heat (above 104°F/40°C) for additional information, see Safety Data Sheet (SDS) if swallowed get medical help or contact a Poison Control Center immediately
🧪 Active Ingredient ▾
Active ingredient Chlorhexidine gluconate solution, 4%
🧪 Inactive Ingredients ▾
Inactive ingredients cocamide DEA, cocamine oxide, fragrance, gluconic acid contains one or more of these ingredients , gluconolactone , hydroxyethyl cellulose, isopropyl alcohol 4%, PEG-75 lanolin, PEG-150 distearate, propylene glycol, quaternium-60, water
🎯 Purpose ▾
Purposes Surgical hand scrub Healthcare personnel handwash Skin wound and general skin cleanser
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
For educational and professional reference only — not medical advice. Pricing reflects published
NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.