hand sanitizer- light pink 01 alcohol 62 mL/100mL Spray, 35 mL — NDC 82953-079-01 (Billing 82953-0079-01)
This is a package of 35 mL of hand sanitizer- light pink 01 alcohol 62 mL/100mL Spray from Cosmuses Cosmetics (Ningbo) Co., Ltd., marketed since Aug 2026 and currently FDA-listed. It is this product's only package size.
NDC database record
One package, one record: these facts belong to NDC 82953-079-01 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 82953 labeler · 079 product · 01 package
- Package marketed since
- Aug 21, 2026
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2027
- Barcode (UPC-A, from the NDC)
- 3 8295307901 3
- FDA record last changed
- Sep 10, 2026
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
- RxCUI (RxNorm): 1020364
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 8, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 8, 2026
RxNorm drug class
This medicine belongs to the Other antiseptics and disinfectants class.
Where does this data come from?
- RxClass (NLM) · catalog refreshed Oct 8, 2026
Clinical
- It depends on the product. Hand sanitizers and wipes help reduce bacteria on your skin, and alcohol pads prepare skin before an injection. A separate injected form is used by heart...
- Most directions say to cover all surfaces of your hands and rub until dry. Sprays and wipes follow similar steps. Check your product's label, since directions differ a bit between...
- Children under 6 should use hand sanitizer only with adult supervision to avoid swallowing. Keep all products out of reach of children. If someone swallows it, get medical help or...
- Stop using it and ask a doctor if you get irritation and redness, or if your condition lasts more than 72 hours. Avoid broken skin and keep it out of your eyes. If it gets in your...
Patient education
Supplement & herbal interactions
Where does this data come from?
- MedlinePlus (NLM) · refreshed Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 2026
Ask a licensed pharmacist directly — free, answered by our team.
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. | |
Where does this data come from?
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 9, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 82953-0079-01 You're viewing this Main listing | 35 mL in 1 VIAL, PLASTIC | 2026-08-21 | — | Active |
Therapeutic equivalents
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file
Availability & generic status
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
- FDA Orange Book · refreshed Oct 3, 2026
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.
🧪 Avoiding an ingredient? See Alcohol inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
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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.
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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 WZB9127XOA
A synthetic red dye used to color medications and make them easier to identify. It serves as a colorant in tablets, capsules, and liquid formulations.
-
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.
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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.
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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.
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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.
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
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.- FDA label on DailyMed · label index refreshed Oct 8, 2026
- FDA openFDA NDC Directory · synced Oct 8, 2026
Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
Why might an inactive ingredient be missing?
Can inactive ingredients matter?
Manufacturer & labeler
More NDCs from Cosmuses Cosmetics (Ningbo) Co., Ltd. labeler code 82953
- lip balm SPF15( 2533) 01 Avobenzone,Homosalate,Octocrylene,Octisalate 5 g/100g; 3 g/100g; 2 g/100g; 3 g/100g Lipstick NDC 82953-073-01
- lip balm SPF15( Zinc oxide) 01 8 g/100g Lipstick NDC 82953-074-01
- hand sanitizer- light green 01 alcohol 62 mL/100mL Spray NDC 82953-075-01
- hand sanitizer- light blue 01 alcohol 62 mL/100mL Spray NDC 82953-076-01
- hand sanitizer- light purple 01 alcohol 62 mL/100mL Spray NDC 82953-077-01
- hand sanitizer- light yellow 01 alcohol 62 mL/100mL Spray NDC 82953-078-01
- SKIN-INFUSED FOUNDATION SPF 25/ Mineral sunscreen broad Spectrum SPF 25 01 Zinc Oxide, Titanium Dioxide 2.7 g/100mL; 16.2 g/100mL Cream NDC 82953-080-01
- SPF30 Sunscreen 01 Avobenzone ,Homosalate,Octocrylene, Octisalate 2.7 g/100mL; 7 g/100mL; 7 g/100mL; 4.5 g/100mL Spray NDC 82953-081-01
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
🎯 Indications and Usage ▾
Uses For hand washing to decrease bacteria on the skin.
⏱️ Dosage and Administration ▾
Directions Wet hands thoroughly and allow to dry without wiping.
⚠️ Warnings ▾
Warnings Flammable. Keep away from fire or flame. For external use only.
📦 Storage and Handling ▾
Other information Store under 104°F/40°C.
🧪 Active Ingredient ▾
Active Ingredients Alcohol 62% v/v
🧪 Inactive Ingredients ▾
Inactive Ingredients Aqua(water), Glycerin, Propylene Glycol, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate, Fragrance(Parfum), FD&C Red No.40(CI 16035).
🎯 Purpose ▾
Purpose Antiseptic
📄 When Using This Product ▾
When using this product , keep out of eyes. In case of contact with eyes, rinse with water.
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask doctor if irritation and redness develops and persists.
📄 Keep Out of Reach of Children ▾
Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.
📄 Package Label / Principal Display Panel ▾
82953-079-01 82953-079-01
About this NDC listing & data coverage
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. |