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hand sanitizer- light yellow 01 alcohol 62 mL/100mL Spray, 35 mL — NDC 82953-0078-01 package photo

hand sanitizer- light yellow 01 alcohol 62 mL/100mL Spray, 35 mL

by Cosmuses Cosmetics (Ningbo) Co., Ltd. · 35 mL in 1 VIAL, PLASTIC (82953-078-01)
NDC 82953-0078-01
🏷️ FDA NDC (as labeled) 82953-078-01 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 10, 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

🆔 Identity & classification

FDA NDC (as labeled) 82953-078-01
Product NDC 82953-078
11-digit billing NDC 82953007801
RxCUI 1020364
UNII 3K9958V90M
Application # M003
SPL Set ID 598bf8cd-2a79-8b56-e063-6394a90a42a8
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-08-21
Route TOPICAL
Dosage form SPRAY
Substance ALCOHOL
Why two NDCs? The FDA registers this code as 82953-078-01 — 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 → 82953-0078-01. 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

LabelerCosmuses Cosmetics (Ningbo) Co., Ltd.
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code82953
First marketedAug 2026
Product typeHuman Otc Drug
Portfolio66 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?
📖 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.

💊 What it looks like

Color yellow
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 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 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 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 I753WB2F1M
    FD&C Yellow No. 5 is a synthetic yellow colorant approved by the FDA. It is added to medicines to make pills, tablets, or liquids visually distinct and easier to identify.
  • UNII 5EM498GW35
    A mixture of aromatic compounds used to add pleasant smell to the medicine. Fragrance helps mask unpleasant tastes or odors, making the medication easier to take.
  • 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.

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

The official label also statesAqua(water), Glycerin, Propylene Glycol, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate, Fragrance(Parfum), FD&C Yellow No.5(CI 19140).

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.
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
Banana Scent Anti Germ 62 mL/100mL 81670-0000-14 F21 14 ml — — FDA listed —
Strawberry Scent Anti Germ 62 mL/100mL 81670-0001-14 F21 14 ml — — FDA listed —
Aloe Vera Scent Anti Germ 62 mL/100mL 81670-0002-14 F21 14 ml — — FDA listed —
Berry Scent Anti Germ 62 mL/100mL 81670-0003-14 F21 14 ml — — FDA listed —
Hand Sanitizer Raspberry Mango 62 mL/100mL 76891-0141-11 SCENT 30 ml — — FDA listed —
Hand Sanitizer Cozy Comfort 62 mL/100mL 76891-0143-11 Scent 30 ml — — FDA listed —
Hand Sanitizer Sun-Kissed Melon 62 mL/100mL 76891-0159-30 Scent 1 bottle — — FDA listed —
Hand Sanitizing Lavender 62 mL/100mL 55814-0101-12 DR. 59 ml — — FDA listed —
Mist 62 mL/100mL 70741-0003-03 Derma 75 ml — — FDA listed —
Solar Flare Hand Sanitizer Brazilian Caramel Dreams 62 mL/100mL 76891-0152-30 Scent 30 ml — — FDA listed —
Scent Theory Hand Sanitizers Cherry Pop, Ocean Splash, Juicy Pear 62 mL/100mL 76891-0168-03 Scent 3 bottles — — FDA listed —
Limited Edition Hand Sanitizer Cherry Chai 62 mL/100mL 76891-0171-30 Scent 1 bottle — — FDA listed —
Boo Crew Hand Care Essentials Boo Berry, Pumpkin Spice 62 mL/100mL 76891-0177-06 Scent 2 bottles — — FDA listed —
Scentfull Midnight Air Hand Sanitizer 62 mL/100mL 76891-0178-35 Scent 1 bottle — — FDA listed —
Lemon Myrtle Hand Sanitizer 62 mL/100mL 52915-0066-19 ORGANIC 562 ml — — FDA listed —
Scent Theory Hand Sanitizer Sprays (Pink Champagne, Harvest Berry, Cozy Coconut) 62 mL/100mL 76891-0146-01 Scent 90 ml — — FDA listed —
Limited Edition Hand Sanitizer Golden Vanilla, Starlight Frost, Pink Satin Prosecco 62 mL/100mL 76891-0174-05 Scent 3 bottles — — FDA listed —
Eucalyptus Ease Hand Sanitizer 62 mL/100mL 52915-0075-19 ORGANIC 562 ml — — FDA listed —
Scentfull Hand Sanitizer Sunrise Glow 62 mL/100mL 76891-0149-35 Scent 35 ml — — FDA listed —
Hand Sanitizer Juicy Pear 62 mL/100mL 76891-0164-02 Scent 1 bottle — — FDA listed —
Limited Edition Hand Sanitizer Cashmere Skin 62 mL/100mL 76891-0169-30 Scent 1 bottle — — FDA listed —
Hand Sanitizer 62 mL/100mL 83986-0199-14 UpLift 162.7 ml — — FDA listed —
Everyone Hand Sanitizer ruby grapefruit 62 mL/100mL 54748-0304-05 EO 59 ml — — FDA listed —
Hand Sanitizer Lush Aloe 62 mL/100mL 76891-0139-11 SCENT 30 ml — — FDA listed —
Hand Sanitizer Rainfall 62 mL/100mL 76891-0140-11 SCENT 30 ml — — FDA listed —
Scentfull Hand Sanitizer Pink Champagne 62 mL/100mL 76891-0147-35 Scent 35 ml — — FDA listed —
Scentfull Hand Sanitizer Sea Breeze 62 mL/100mL 76891-0151-35 Scent 35 ml — — FDA listed —
Solar Flare Hand Sanitizer Sunset Samba 62 mL/100mL 76891-0153-30 Scent 30 ml — — FDA listed —
Hand Sanitizer Ocean Mist 62 mL/100mL 76891-0156-30 Scent 1 bottle — — FDA listed —
Hand Sanitizer Banana Creme 62 mL/100mL 76891-0163-02 Scent 1 bottle — — FDA listed —
Scentfull Hand Sanitizer Eucalyptus Aloe 62 mL/100mL 76891-0148-35 Scent 35 ml — — FDA listed —
Solar Flare Hand Sanitizer Set Sea Veil, Pink Glow, Coco Creme 62 mL/100mL 76891-0154-01 Scent 3 pouches — — FDA listed —
Scent Theory Hand Sanitizer (Peach Peony, Dragonfruit Paradise, Coastal Fleur) 62 mL/100mL 76891-0160-01 Scent 3 bottles — — FDA listed —
Hand Sanitizer Pink Melon 62 mL/100mL 76891-0166-02 Scent 1 bottle — — FDA listed —
Limited Edition Hand Sanitizer Pink Satin Prosecco 62 mL/100mL 76891-0170-30 Scent 1 bottle — — FDA listed —
Elf Hand Sanitizer Gift Set Maple Syrup Drizzle, Peppermint Sugar Rush, Creamy Vanilla Swirl 62 mL/100mL 76891-0179-05 Scent 3 bottles — — FDA listed —
EO HAND SANITIZER Lavender 62 mL/100mL 54748-0101-01 EO 10 ml — — Discontinued —
Hand Sanitizer Brazilian Coconut 62 mL/100mL 76891-0138-11 SCENT 30 ml — — Discontinued —
everyone Hand Sanitizer Coconut Lemon 62 mL/100mL 54748-0301-05 EO 59 ml — — FDA listed —
Organic Hand Sanitizer Peppermint 62 mL/100mL 55814-0102-12 DR. 59 ml — — FDA listed —
Hand Sanitizer Sandalwood Waves 62 mL/100mL 76891-0142-11 SCENT 30 ml — — FDA listed —
Hand Sanitizer Whipped Chai 62 mL/100mL 76891-0144-11 Scent 30 ml — — FDA listed —
Scent Theory Hand Sanitizer Sprays (Blissful Cherry, Candy Cane Cocoa, Molten Marshmallows) 62 mL/100mL 76891-0145-01 Scent 90 ml — — FDA listed —
Hand Sanitizer Velvet Vanilla 62 mL/100mL 76891-0158-30 Scent 1 bottle — — FDA listed —
Calming Hand Sanitizer 62 mL/100mL 52915-0074-19 ORGANIC 562 ml — — FDA listed —
Scentfull Hand Sanitizer Whipped Coconut 62 mL/100mL 76891-0150-35 Scent 35 ml — — FDA listed —
Hand Sanitizer Matcha Mood 62 mL/100mL 76891-0155-30 Scent 1 bottle — — FDA listed —
Hand Sanitizer Sunrise Citrus 62 mL/100mL 76891-0157-30 Scent 1 bottle — — FDA listed —
Hand Sanitizer Cherry Pop 62 mL/100mL 76891-0162-02 Scent 1 bottle — — FDA listed —
Hand Sanitizer Ocean Splash 62 mL/100mL 76891-0165-02 Scent 1 bottle — — FDA listed —
hand sanitizer 01 62 mL/100mL 82953-0021-01 Cosmuses 10 ml — — FDA listed —
Everyone Hand Sanitizer Lavender Aloe 62 mL/100mL 54748-0303-03 EO 3 bottles — — Discontinued —
Scent Theory Hand Sanitizers Coastal Mist, Boardwalk Treats, Firecracker Freeze 62 mL/100mL 76891-0161-01 Scent 3 bottles — — FDA listed —
Scentfull Hand Sanitizer Pink Champagne 62 mL/100mL 76891-0181-35 Scent 1 bottle — — FDA listed —
Scentfull Hand Sanitizer Blue Driftwood 62 mL/100mL 76891-0180-35 Scent 1 bottle — — FDA listed —
Twisted Caramel Apple Hand Sanitizer 62 mL/100mL 76891-0183-07 Scent 1 bottle — — FDA listed —
Molten Marshmallow Hand Sanitizer 62 mL/100mL 76891-0184-07 Scent 1 bottle — — FDA listed —
Midnight Magic Hand Sanitizer 62 mL/100mL 76891-0182-07 Scent 1 bottle — — FDA listed —
hand sanitizer 01 62 mL/100mL 82953-0071-01 Cosmuses 20 ml — — FDA listed —
It Bag Strawberry Love Hand Sanitizer 62 mL/100mL 76891-0187-07 Scent 1 bottle — — FDA listed —
It Bag Vanilla Sugar Hand Sanitizer 62 mL/100mL 76891-0185-07 Scent 1 bottle — — FDA listed —
It Bag Cherry Kiss Hand Sanitizer 62 mL/100mL 76891-0186-07 Scent 1 bottle — — FDA listed —
hand sanitizer- light purple 01 62 mL/100mL 82953-0077-01 Cosmuses 35 ml — — FDA listed —
hand sanitizer- light yellow 01 62 mL/100mLthis 82953-0078-01 Cosmuses 35 ml — — FDA listed —
hand sanitizer- light pink 01 62 mL/100mL 82953-0079-01 Cosmuses 35 ml — — FDA listed —
hand sanitizer- light blue 01 62 mL/100mL 82953-0076-01 Cosmuses 35 ml — — FDA listed —
hand sanitizer- light green 01 62 mL/100mL 82953-0075-01 Cosmuses 35 ml — — FDA listed —
Sweethearts - Crush On You - Peach Skin 62 mL/100mL 76891-0188-07 Scent 1 bottle — — FDA listed —
Sweethearts - Be Mine - Sugared Berries 62 mL/100mL 76891-0189-07 Scent 1 bottle — — FDA listed —
Sweethearts - Ooo La La - Banana Cream Hand Sanitizer 62 mL/100mL 76891-0191-07 Scent 1 bottle — — FDA listed —
Sweethearts - UR Sweet - Sweet Cherry Hand Sanitizer 62 mL/100mL 76891-0190-07 Scent 1 bottle — — 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

🏛️
2026
On the market since
Aug 2026
📍
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
82953-0078-01 You're viewing this 35 mL in 1 VIAL, PLASTIC (82953-078-01) 2026-08-21 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product
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.
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 82953-078-01, 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: 82953-0078-01, written without dashes as 82953007801. 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 82953-0078-01, the first segment (82953) is the labeler code FDA assigned to Cosmuses Cosmetics (Ningbo) Co., Ltd.; the middle segment (0078) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Cosmuses Cosmetics (Ningbo) Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Cosmuses Cosmetics (Ningbo) Co., Ltd. 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 10 words ▾

Uses For hand washing to decrease bacteria on the skin.

⏱️ Dosage and Administration 10 words ▾

Directions Wet hands thoroughly and allow to dry without wiping.

⚠️ Warnings 12 words ▾

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

📦 Storage and Handling 6 words ▾

Other information ​ Store under 104°F/40°C.

🧪 Active Ingredient 5 words ▾

Active Ingredients Alcohol 62% v/v

🧪 Inactive Ingredients 17 words ▾

Inactive Ingredients Aqua(water), Glycerin, Propylene Glycol, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate, Fragrance(Parfum), FD&C Yellow No.5(CI 19140).

🎯 Purpose 2 words ▾

Purpose Antiseptic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 82953-0077-01 · Cosmuses 82953-0079-01 · Cosmuses →
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.