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Hand Sanitizer ALCOHOL 75 mL/100mL Aerosol, Spray — NDC 58133-0959-73 package photo

Hand Sanitizer ALCOHOL 75 mL/100mL Aerosol, Spray

by Cosmetic Specialty Labs, Inc. · 1 BOTTLE in 1 BOX (58133-959-73) / 178 mL in 1 BOTTLE (58133-959-70)
NDC 58133-0959-73
🏷️ FDA NDC (as labeled) 58133-959-73 billing pads the product segment with a zero
This package
Contains178 mL in 1 bottle Pack sizes18 compare ↓
Also comes in: 178 mL 58133-0959-71 178 mL 58133-0959-72 15 ml 58133-0959-16 15 ml 58133-0959-17 15 ml 58133-0959-18 15 ml 58133-0959-20 15 ml 58133-0959-15 15 ml 58133-0959-21 15 ml 58133-0959-19 178 ml 58133-0959-60 178 ml 58133-0959-61 178 ml 58133-0959-62 178 ml 58133-0959-63 178 ml 58133-0959-64 178 ml 58133-0959-66 178 ml 58133-0959-65 178 ml 58133-0959-67
OTC Discontinued Non-controlled ⚠ Inactivated by FDA
🗂️ Data synced Jul 14, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

⚠️
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 2024. 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) 58133-959-73
Product NDC 58133-959
11-digit billing NDC 58133095973
Application # part333A
SPL Set ID bf3eceb7-aed8-337b-e053-2995a90ace41
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH NOT FINAL
Marketing status Discontinued
FDA listing status Inactivated by FDA (certified through Dec 2024)
Route TOPICAL
Dosage form AEROSOL, SPRAY
Substance ALCOHOL
Why two NDCs? The FDA registers this code as 58133-959-73 — 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 → 58133-0959-73. 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.

🏭 Manufacturer & labeler

LabelerCosmetic Specialty Labs, Inc.
FDA applicationpart333A (OTC MONOGRAPH NOT FINAL)
Labeler code58133
Product typeHuman Otc Drug
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?
📖 Read our full Alcohol guide →

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
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.

🧪 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 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII 00YIU5438U
    Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
  • 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 HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • 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.

7 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesAloe Barbadensis Leaf Juice, Caprylyl Glycol, Fragrance, Glycerin, Phenoxyethanol, Polysorbate-20, Purified Water, Tocopheryl Acetate.

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 systemPer mLPer 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
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size: 178 mL 178 mL 15 ml 15 ml 15 ml 15 ml 15 ml 15 ml 15 ml 178 ml 178 ml 178 ml 178 ml 178 ml 178 ml 178 ml 178 ml
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

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Hand Sanitizer 75 mL/100mLthis 58133-0959-73 Cosmetic 1 bottle — — Discontinued —
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

📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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

Completed Suicide8,244
Toxicity To Various Agents7,784
Drug Abuse6,958
Death2,735
Overdose2,330
Cardio-respiratory Arrest2,150
Intentional Overdose1,955

Age at onset

Neonate26
Infant16
Child17
Adolescent102
Adult3,298
Elderly329

Reporter sex

35,235 reports
Male · 54%
Female · 46%
Unknown · 0%

Serious outcomes

Death22,164
Hospitalization9,875
Life-threatening1,623
Disabling246
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 2,706 0
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 NDCDescription Marketing startStatus
58133-0959-16 15 mL in 1 BOTTLE, PUMP (58133-959-16) 2021-04-05 Inactivated by FDA
58133-0959-17 15 mL in 1 BOTTLE, PUMP (58133-959-17) 2021-04-05 Inactivated by FDA
58133-0959-18 15 mL in 1 BOTTLE, PUMP (58133-959-18) 2021-04-05 Inactivated by FDA
58133-0959-60 178 mL in 1 BOTTLE, PUMP (58133-959-60) 2021-08-30 Inactivated by FDA
58133-0959-61 178 mL in 1 BOTTLE, PUMP (58133-959-61) 2021-08-30 Inactivated by FDA
58133-0959-62 178 mL in 1 BOTTLE, PUMP (58133-959-62) 2021-08-30 Inactivated by FDA
58133-0959-63 178 mL in 1 BOTTLE, PUMP (58133-959-63) 2021-08-30 Inactivated by FDA
58133-0959-64 178 mL in 1 BOTTLE, PUMP (58133-959-64) 2021-08-30 Inactivated by FDA
58133-0959-66 178 mL in 1 BOTTLE, PUMP (58133-959-66) 2021-08-30 Inactivated by FDA
58133-0959-65 178 mL in 1 BOTTLE, PUMP (58133-959-65) 2021-08-30 Inactivated by FDA
58133-0959-67 178 mL in 1 BOTTLE, PUMP (58133-959-67) 2021-08-30 Inactivated by FDA
58133-0959-71 1 BOTTLE in 1 BOX (58133-959-71) / 178 mL in 1 BOTTLE (58133-959-68) 2023-05-03 Inactivated by FDA
58133-0959-20 15 mL in 1 BOTTLE, SPRAY (58133-959-20) 2023-05-03 Inactivated by FDA
58133-0959-15 15 mL in 1 BOTTLE, SPRAY (58133-959-15) 2023-05-03 Inactivated by FDA
58133-0959-73 You're viewing this 1 BOTTLE in 1 BOX (58133-959-73) / 178 mL in 1 BOTTLE (58133-959-70) 2023-05-03 Inactivated by FDA
58133-0959-72 1 BOTTLE in 1 BOX (58133-959-72) / 178 mL in 1 BOTTLE (58133-959-69) 2023-05-03 Inactivated by FDA
58133-0959-21 15 mL in 1 BOTTLE, SPRAY (58133-959-21) 2023-05-03 Inactivated by FDA
58133-0959-19 15 mL in 1 BOTTLE, SPRAY (58133-959-19) 2023-05-03 Inactivated by FDA

Pack size FAQ

What quantity is in NDC 58133-0959-73?
NDC 58133-0959-73 is listed by the FDA — 1 bottle in 1 box / 178 ml in 1 bottle.
What NDC number is used to bill for this package of Hand Sanitizer ALCOHOL 75 mL/100mL Aerosol, Spray?
Bill NDC 58133-0959-73 — the 11-digit billing format is 58133095973. 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 Not Final". 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 58133-959-73, 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: 58133-0959-73, written without dashes as 58133095973. 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 58133-0959-73, the first segment (58133) is the labeler code FDA assigned to Cosmetic Specialty Labs, Inc.; the middle segment (0959) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (73) 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 17 other package presentations of this same product, including 1 bottle (58133-0959-71), 1 bottle (58133-0959-72), 15 ml (58133-0959-16). 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?
Cosmetic Specialty Labs, 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 24 words ▾

Use Hand Sanitizer to help reduce bacteria on the skin. Use subsection identifying number is Sequence 4. change incorporated in the label on 4/2021.

⏱️ Dosage and Administration 43 words ▾

Directions Use enough product in your palm to cover hands and rub hands together biskly until dry. Children under 6 years of age should be supervised when using this product. Directions Identifying number of subsection is 9. change incorporated in the label 04/2021.

⚠️ Warnings 12 words ▾

Warnings Flammable. Keep away from fire or flame. For external use only.

📦 Storage and Handling 11 words ▾

Other information Store below 110F (43C) May discolor fabrics or surfaces

🧪 Active Ingredient 6 words ▾

Active Ingredient SD Alcohol 40 75%

🧪 Inactive Ingredients 16 words ▾

Inactive ingredients Aloe Barbadensis Leaf Juice, Caprylyl Glycol, Fragrance, Glycerin, Phenoxyethanol, Polysorbate-20, Purified Water, Tocopheryl Acetate.

🎯 Purpose 1 words ▾

Antimicrobial

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 58118-8815-08 · Clinical 58135-0001-00 · Huatai →
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.