Hand Sanitizer Ethanol 70 mL/100mL Liquid, 2400 mL
by Tazza Brands East Inc. · 2400 mL in 1 BOTTLE, PLASTIC (76370-0005-6)
NDC 76370-0005-06
🏷️ FDA NDC (as labeled)
76370-0005-6
billing pads the package segment with a zero
This package
Contains2400 mL
Pack sizes4 compare ↓
OTC
Discontinued
Non-controlled
⚠ Inactivated by FDA
🗂️ 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 →
⚠️
Other active recalls for Ethanol (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · May 22, 2026 — Microbial contamination of sterile products (Zep Inc) · FDA recall D-0586-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗
⚠️
Excluded from the active FDA NDC Directory.
FDA inactivated this product’s listing record, so it is excluded from the active NDC Directory. The listing was last certified through Dec 2026. 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)
76370-0005-6
Product NDC
76370-0005
11-digit billing NDC
76370000506
RxCUI
616805
UNII
3K9958V90M
Application #
505G(a)(3)
SPL Set ID
464f97a0-6263-224f-e054-00144ff8d46c
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
Discontinued
FDA listing status
Inactivated by FDA (certified through Dec 2026)
Marketing start
2017-01-17
Route
TOPICAL
Dosage form
LIQUID
Substance
ALCOHOL
Why two NDCs?
The FDA registers this code as 76370-0005-6 — a 5-4-1 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 package segment → 76370-0005-06. 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 Other antiseptics and disinfectants class.
Drug family (ATC)
Other antiseptics and disinfectants, Antidotes, Nerve depressants
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
LabelerTazza Brands East Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code76370
First marketedJan 2017
Product typeHuman Otc Drug
Portfolio22 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
- Chemically they are related, but hand sanitizer is absolutely not safe to drink — it contains alcohol in concentrations that are toxic if swallowed and often includes other ingredi...
- Is the alcohol in hand sanitizer the same as the alcohol in a drink?
- Yes — most of these products are specifically labeled 'recommended for repeated use.' Just apply enough to cover your hands and rub until dry. If you notice skin irritation or redn...
- Can I use hand sanitizer over and over throughout the day?
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Ethanol — tap one for details:
4
Nutrient depletion considerations
Ethanol may be associated with lower levels of 4 nutrients — worth a chat with your pharmacist, not a cause for alarm.
VITAMIN C
Insignificant Depletion
FOLIC ACID
Moderate Depletion
GLUTATHIONE
Insufficient Evidence
ZEAXANTHIN
Insufficient Evidence
An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
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 Ethanol?
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 ZY81Z83H0X
Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
-
UNII AZE05TDV2V
Diethanolamine is a chemical compound used in medicines as a pH adjuster and emulsifier. It helps balance acidity levels and allows oils and water-based ingredients to mix smoothly in liquid formulations.
-
UNII PDC6A3C0OX
Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
-
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 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.
5 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesInactive ingredients Purified Water, Diethanolamine, Propylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice.
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 |
|---|---|---|---|---|---|---|
| PURELL Advanced E3 Rated Instant Hand Sanitizer Foam .7 mL/mL 21749-0802-51 | GOJO | 550 ml | — | — | Discontinued | — |
| PURELL Advanced Green Certified Instant Hand Sanitizer .7 mL/mL 21749-0806-51 | GOJO | 550 ml | — | — | Discontinued | — |
| PURELL Advanced Instant Hand Sanitizer .7 mL/mL 21749-0807-17 | GOJO | 515 ml | — | — | FDA listed | — |
| PURELL Healthcare Advanced Hand Sanitizer Foam .7 mL/mL 21749-0811-45 | GOJO | 450 ml | — | — | Discontinued | — |
| PURELL Healthcare Advanced Hand Sanitizer Gentle and Free Foam .7 mL/mL 21749-0822-53 | GOJO | 535 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer Gentle and Free Foam .7 mL/mL 21749-0826-53 | GOJO | 535 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer Fragrance Free Foam .7 mL/mL 21749-0827-17 | GOJO | 515 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer Moisturizing 2in1 Foam 70 mL/100mL 21749-0851-10 | GOJO | 295 ml | — | — | FDA listed | — |
| PURELL Healthcare Advanced Hand Sanitizer ULTRA NOURISHING Foam .7 mL/mL 21749-0854-53 | GOJO | 535 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer ULTRA NOURISHING Foam 70 mL/100mL 21749-0856-17 | GOJO | 515 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer Naturals Foam 70 mL/100mL 21749-0875-10 | GOJO | 295 ml | — | — | FDA listed | — |
| Symmetry Foaming Hand Sanitizer Fragrance Free 70 mL/100mL 30805-0020-04 | Buckeye | 1200 ml | — | — | FDA listed | — |
| Symmetry Foaming Hand Sanitizer 70 mL/100mL 30805-0021-09 | Buckeye | 1000 ml | — | — | FDA listed | — |
| Altra Foaming Hand Sanitizer Fragrance Free with Aloe and Vitamin E 70 mL/100mL 30805-0023-07 | Buckeye | 550 ml | — | — | FDA listed | — |
| I-70 Foaming .7 mL/mL 43097-0968-12 | People's | 1000 ml | — | — | FDA listed | — |
| ESC Protecting Foam Hand Sanitizer 76.9 mL/100mL 47593-0667-41 | Ecolab | 750 ml | — | — | FDA listed | — |
| Ecolab Retail Foaming Alcohol Hand Sanitizer 70 mL/100mL 47593-0685-56 | Ecolab | 1200 ml | — | — | FDA listed | — |
| Kay Alcohol Foam Hand Sanitizer 70 mL/100mL 47593-0686-56 | Ecolab | 1200 ml | — | — | FDA listed | — |
| Tork Hand Sanitizing Alcohol Foam 70 mL/100mL 49351-0301-01 | Essity | 1000 ml | — | — | FDA listed | — |
| Foaming Hand Sanitizer 70 mL/100mL 50021-0020-01 | Empack | 550 ml | — | — | FDA listed | — |
| MG FoamSan 70 .7 L/L 50241-0223-02 | Morgan | 3.785 l | — | — | FDA listed | — |
| EnMotion Foam Hand Sanitizer 70 mL/100mL 54622-0120-01 | Georgia-Pacific | 1000 ml | — | — | FDA listed | — |
| enMotion Foam High Frequency Use .7 mL/mL 54622-0121-01 | Georgia-Pacific | 2 bottles | — | — | FDA listed | — |
| Pacific Blue Ultra Foaming Fragrance Free 70 mg/mL 54622-0122-01 | Georgia-Pacific | 1000 ml | — | — | FDA listed | — |
| Pacific Blue Select Foam Hand Sanitizer, Fragrance Free, Dye Free 70 mL/100mL 54622-0311-01 | Georgia-Pacific | 24 bottles | — | — | FDA listed | — |
| enMotion Foam High Frequency Use 70 mL/100mL 54622-0486-01 | Georgia-Pacific | 1000 ml | — | — | FDA listed | — |
| Kleenex Ultra Moisturizing Hand Sanitizer 70 mL/100mL 55118-0530-10 | Kimberly-Clark | 1000 ml | — | — | Discontinued | — |
| Kleenex Reveal Moisturizing Foam Hand Sanitizer 70 mL/100mL 55118-0531-10 | Kimberly-Clark | 6 bottles | — | — | Discontinued | — |
| Lynx san a foam .7 mL/mL 62257-0007-10 | ABC | 1000 ml | — | — | FDA listed | — |
| Fast .7 mL/mL 62257-0658-08 | ABC | 1000 ml | — | — | Discontinued | — |
| Dermacen Foaming Instant Hand Sanitizer With Aloe 70 mL/100mL 62654-0149-13 | Central | 1000 ml | — | — | FDA listed | — |
| Saniclean 70 g/100mL 63900-0150-02 | Simoniz | 1000 ml | — | — | FDA listed | — |
| Foaming Instant Hand Sanitizer with Aloe 70 g/100g 68599-5205-01 | MCKESSON | 251 g | — | — | FDA listed | — |
| Hand Sanitizer 70 mL/100mL 69790-0456-44 | Uline | 532 ml | — | — | FDA listed | — |
| EXTENDED CARE Foaming Hand Sanitizer .7 mL/mL 71875-0800-40 | TRIPLE | 1200 ml | — | — | FDA listed | — |
| Hand Sanitizer 70 mL/100mL 71897-0465-86 | Veritiv | 1000 ml | — | — | FDA listed | — |
| Clean Revolution Foaming Hand Sanitizer Refill Supply Container - Gentle and Aloe Enriched - ELIMINATES 99.9% Germs - 70% Ethanol - Ready To Use 70 mL/100mL 74810-0725-00 | Replenish | 3785 ml | — | — | FDA listed | — |
| Recens Foam .7 mL/mL 75990-0968-07 | Certus | 700 ml | — | — | Discontinued | — |
| Hand Sanitizer 70 mL/100mL 76370-0003-01 | Tazza | 10000 ml | — | — | Discontinued | — |
| Hand Sanitizer 70 mL/100mLthis 76370-0005-06 | Tazza | 2400 ml | — | — | Discontinued | — |
| Tazza 70% Alcohol-Based Hand Sanitizing Foam 70 L/100L 76370-0033-00 | Tazza | 3.785 l | — | — | FDA listed | — |
| Hand Sanitizer Foam 70 mL/100mL 77955-0002-02 | Custom | 1000 ml | — | — | FDA listed | — |
| Ops 70 Percent Alcohol Foaming Skin Sanitizer 70 mL/100mL 79016-0101-12 | Archer | 1000 ml | — | — | FDA listed | — |
| Black Ops 70 Percent Alcohol Foaming Skin Sanitizer 70 mL/100mL 79016-0102-12 | Archer | 1000 ml | — | — | FDA listed | — |
| KleenLine Essentials Foaming Hand Sanitizer .7 mL/mL 79258-0802-29 | Brady | 1000 ml | — | — | FDA listed | — |
| MyHealth Advanced Hand Sanitizer 70 mL/100mL 80661-0002-01 | Aeroflex | 150 ml | — | — | FDA listed | — |
| Novo Foaming Instant Hand Sanitizer .7 mL/mL 81551-0802-04 | Noble | 3785 ml | — | — | FDA listed | — |
| Foaming Hand Alcohol Foam 70 mL/100mL 83019-0102-11 | Draco | 1000 ml | — | — | FDA listed | — |
| AFCO 5511 Sanifect E3 70 mL/100mL 66949-0140-01 | Zep | 208198 ml | — | — | FDA listed | — |
| Hand Sanitizer Gel 70 mL/100mL 66949-0137-08 | Zep | 2840 ml | — | — | FDA listed | — |
| Zep Alcohol Sanitizer 70 mL/100mL 66949-0133-01 | Zep | 11400 ml | — | — | FDA listed | — |
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
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
🏛️
2017
On the market since
Jan 2017
📍
2026
Currently FDA-listed
9 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found
We did not find an FDA-approved generic match for this exact strength, form and route.
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.
🔬 Reported adverse events (FAERS)
Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for HAND SANITIZER (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 54%
Female · 46%
Unknown · 0%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 76370-0005-02 | 3785 mL in 1 BOTTLE, SPRAY (76370-0005-2) | 2020-07-02 | Inactivated by FDA |
| 76370-0005-04 | 946 mL in 1 BOTTLE, SPRAY (76370-0005-4) | 2020-07-02 | Inactivated by FDA |
| 76370-0005-05 | 1000 mL in 1 BOTTLE, PLASTIC (76370-0005-5) | 2017-01-17 | Inactivated by FDA |
| 76370-0005-06 You're viewing this | 2400 mL in 1 BOTTLE, PLASTIC (76370-0005-6) | 2017-01-17 | Inactivated by FDA |
You're viewing one of 4 pack sizes for this product.
Pack size FAQ
What quantity is in NDC 76370-0005-06?
NDC 76370-0005-06 contains 2400 mL — 2400 ml in 1 bottle, plastic.
What is the difference between NDC 76370-0005-06 and NDC 76370-0005-04?
Both are Hand Sanitizer Ethanol 70 mL/100mL Liquid — the drug itself is identical. NDC 76370-0005-06 is the 2400 mL package, while NDC 76370-0005-04 is the 946 ml package.
What NDC number is used to bill for this package of Hand Sanitizer Ethanol 70 mL/100mL Liquid?
Bill NDC 76370-0005-06 — the 11-digit billing format is 76370000506. 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
Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
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 76370-0005-6, 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: 76370-0005-06, written without dashes as 76370000506. 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 76370-0005-06, the first segment (76370) is the labeler code FDA assigned to Tazza Brands East Inc.; the middle segment (0005) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (06) 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 946 ml (76370-0005-04), 1000 ml (76370-0005-05), 3785 ml (76370-0005-02). 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?
Tazza Brands East 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 for hand sanitizing to decrease bacteria on the skin recommended for repeated use
⏱️ Dosage and Administration ▾
Directions apply liberally into palm of hand rub hands together until dry no need to rinse
⚠️ Warnings ▾
Warnings For external use only Flammable. Keep away from fire or flame.
📦 Storage and Handling ▾
Other information do not store above 100°F (38°C) non-staining may discolor some fabrics
🧪 Active Ingredient ▾
Active ingredient Ethanol 70%
🧪 Inactive Ingredients ▾
Inactive ingredients Purified Water, Diethanolamine, Propylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice.
🎯 Purpose ▾
Purpose Antiseptic
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.