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CoreTex Antibacterial Hand Sanitizer SD alcohol 70 mL/100mL Liquid, 30 mL — NDC 65753-0201-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

CoreTex Antibacterial Hand Sanitizer SD alcohol 70 mL/100mL Liquid, 30 mL — NDC 65753-201-01 (Billing 65753-0201-01)

by CoreTex Products Inc · 30 mL in 1 BOTTLE

This is a package of 30 mL of CoreTex Antibacterial Hand Sanitizer SD alcohol 70 mL/100mL Liquid from CoreTex Products Inc, marketed since Jan 2024 and currently FDA-listed. It is the main listing for this product, which comes in 14 package sizes.

NDC 65753-0201-01
🏷️ FDA NDC (as labeled) 65753-201-01 billing pads the product segment with a zero
This package
Contains30 mL Pack sizes14 compare ↓
Main listing for product 65753-201 · Also comes in: 25 pouches 65753-201-20 44 ml 65753-201-32 59 ml 65753-201-02 118 ml 65753-201-03 118 ml 65753-201-28 237 ml 65753-201-05 237 ml 65753-201-29 300 pouches 65753-201-21 354 ml 65753-201-07 355 ml 65753-201-06 473 ml 65753-201-30 750 ml 65753-201-35 3800 ml 65753-201-10
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 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

NDC database record

One package, one record: these facts belong to NDC 65753-201-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
65753 labeler · 201 product · 01 package
Package marketed since
Jan 1, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0698229236128, 0698229236661, 0698229236623, 0698229236166 +5 more
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 65753-201-01
Product NDC 65753-201
11-digit billing NDC 65753020101
RxCUI 582753
UNII 3K9958V90M
UPC 0698229236128, 0698229236661, 0698229236623, 0698229236166 +5 more
Application # M003
SPL Set ID 136d8fe4-df26-c292-e063-6394a90afbec
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-01-01
Route TOPICAL
Dosage form LIQUID
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 582753
Why two NDCs? The FDA registers this code as 65753-201-01 — 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 → 65753-0201-01. 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.

Clinical

📗 Our plain-language guide HelloPharmacist
  • 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...
📖 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.

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: 25 pouches 44 ml 59 ml 118 ml 118 ml 237 ml 237 ml 300 pouches 354 ml 355 ml 473 ml 750 ml 3800 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
65753-0201-01 You're viewing this Main listing 30 mL in 1 BOTTLE 2024-01-01 — Active
65753-0201-02 65753-201-02 59 mL in 1 BOTTLE 2024-01-01 — Active
65753-0201-03 65753-201-03 118 mL in 1 BOTTLE 2024-01-01 — Active
65753-0201-05 65753-201-05 237 mL in 1 BOTTLE 2024-01-01 — Active
65753-0201-06 65753-201-06 355 mL in 1 BOTTLE 2024-01-01 — Active
65753-0201-07 65753-201-07 354 mL in 1 BOTTLE, PUMP 2024-01-01 — Active
65753-0201-10 65753-201-10 3800 mL in 1 BOTTLE 2024-01-01 — Active
65753-0201-20 65753-201-20 25 POUCH in 1 CONTAINER / 3.5 mL in 1 POUCH 2024-01-01 — Discontinued by firm
65753-0201-21 65753-201-21 300 POUCH in 1 CONTAINER / 3.5 mL in 1 POUCH 2024-01-01 — Discontinued by firm
65753-0201-28 65753-201-28 118 mL in 1 BOTTLE, PUMP 2024-01-01 — Active
65753-0201-29 65753-201-29 237 mL in 1 BOTTLE, PUMP 2024-01-01 — Active
65753-0201-30 65753-201-30 473 mL in 1 BOTTLE, PUMP 2024-01-01 — Active
65753-0201-32 65753-201-32 44 mL in 1 BOTTLE 2024-01-01 — Active
65753-0201-35 65753-201-35 750 mL in 1 BOTTLE 2024-01-01 — Active

Pack size FAQ

What quantity is in this package?
This package contains 30 mL — 30 ml in 1 bottle.
How does this package differ from NDC 65753-0201-20?
Both are CoreTex Antibacterial Hand Sanitizer SD alcohol 70 mL/100mL Liquid — the drug itself is identical. This page's package is the 30 mL one, while NDC 65753-0201-20 is the 25 pouches package.
What NDC number is used to bill for this package of CoreTex Antibacterial Hand Sanitizer SD alcohol 70 mL/100mL Liquid?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Ethyl Rubbing Alcohol 70 mL/100mL 70000-0020-01 Cardinal 473 ml $0.004 — Availability likely —
Ethyl alcohol 70 mL/100mL 70677-1220-01 Strategic 473 ml $0.004 — Availability likely —
Ethyl Rubbing Alcohol 70 mL/100mL 00363-0876-43 Walgreen 473 ml — — FDA listed —
Ethyl Rubbing Alcohol 700 mg/mL 00395-0040-16 Humco 473 ml — — FDA listed —
Rubbing 70 mL/100mL 00869-0876-43 Nice-Pak 473 ml — — FDA listed —
Alcare Antiseptic Handrub 70 mL/100mL 11084-0035-18 SC 370 ml — — FDA listed —
Ethyl Alcohol 70 mL/100mL 11344-0876-43 Nice-Pak 473 ml — — FDA listed —
Signature Select Advanced Hand Sanitizer with Aloe Vera 70 mL/100mL 21130-0066-01 Living 59 ml — — FDA listed —
Signature Select Advanced Hand Sanitizer 70 mL/100mL 21130-0077-01 Living 59 ml — — FDA listed —
PURELL Advanced Instant Hand Sanitizer .7 mL/mL 21749-0700-00 GOJO 1.2 ml — — Discontinued —
PURELL Waterless Surgical Scrub .7 mL/mL 21749-0992-02 GOJO 59 ml — — FDA listed —
Rubbing 70 mL/100mL 41163-0876-43 United 473 ml — — FDA listed —
Rubbing 70 mL/100mL 50804-0876-43 Perrigo 473 ml — — FDA listed —
DOP Ethyl Alcohol 70% 70 mL/100mL 51048-0048-16 Omega 473 ml — — FDA listed —
INSTANT HAND SANITIZER Classic 70 mL/100mL 52000-0434-01 Universal 1000 ml — — FDA listed —
Ethyl Rubbing Alcohol 70 mL/100mL 55301-0876-43 Your 473 ml — — FDA listed —
Hand sanitizer 8oz with vitamin E 70 mL/100mL 55319-0116-01 Midwood 236 ml — — FDA listed —
Hand sanitizer 8oz with aloe vera 70 mL/100mL 55319-0117-01 Midwood 236 ml — — FDA listed —
Hand sanitizer 16.9oz with vitamin E 70 mL/100mL 55319-0118-01 Midwood 500 ml — — FDA listed —
Instant Hand Sanitizer 2oz Bonus pack 70 mL/100mL 57337-0093-01 Rejoice 59 ml — — FDA listed —
Hand Sanitizer w/ Carabiner (Strawberry Scented) 2oz Bonus pack 70 mL/100mL 57337-0094-01 Rejoice 2 bottles — — FDA listed —
Hand Sanitizer w/ Carabiner (Lemon Scented) 2oz Bonus pack 70 mL/100mL 57337-0095-01 Rejoice 2 bottles — — FDA listed —
Hand Sanitizer w/ Carabiner (Watermelon Scented) 2oz Bonus pack 70 mL/100mL 57337-0096-01 Rejoice 2 bottles — — FDA listed —
Hand Sanitizer 1.8 oz Antiseptic 70 mL/100mL 57337-0107-01 REJOICE 1 bottle — — FDA listed —
Hand Sanitizer 1.8 oz Lemon Ice 70 mL/100mL 57337-0110-01 Ningbo 53 ml — — FDA listed —
Hand Sanitizer 1.8 oz Watermelon Scented 1.8 oz. 70 mL/100mL 57337-0111-01 Ningbo 53 ml — — FDA listed —
Hand Sanitizer 1.8 oz Strawberry Scented 70 mL/100mL 57337-0112-01 Ningbo 53 ml — — FDA listed —
Hand Sanitizer Vitamin E and Aloe Vera 2 oz. 2 pk 70 mL/100mL 57337-0114-01 Ningbo 2 bottles — — FDA listed —
Hand Sanitizer 8 oz. Vitamin E 70 v/v 70 mL/100mL 57337-0115-01 Ningbo 236 ml — — FDA listed —
Hand Sanitizer Vitamin E and Aloe Vera 70 mL/100mL 57337-0116-01 Ningbo 236 ml — — FDA listed —
Hand Sanitizer Original 1.8 oz 70 mL/100mL 57337-0117-01 Ningbo 53 ml — — FDA listed —
Hand Sanitizer Antibacterial Vitamin E 2 oz. 2 pk 70 mL/100mL 57337-0118-01 Ningbo 2 bottles — — FDA listed —
Hand Sanitizer Vitamin E 70 mL/100mL 57337-0119-01 Ningbo 2 bottles — — FDA listed —
Hand Sanitizer Antibacterial Vitamin E 70 mL/100mL 57337-0120-01 Ningbo 500 ml — — FDA listed —
Hand Sanitizer Antibacterial Vitamin E 70 mL/100mL 57337-0121-01 Ningbo 177 ml — — FDA listed —
Hand Sanitizer Antibacterial Vitamin E 70 mL/100mL 57337-0122-01 Ningbo 1000 ml — — FDA listed —
Hand Sanitizer 2pk Lemon 2oz 70 mL/100mL 57337-0123-01 Ningbo 1 bottle — — FDA listed —
Hand Sanitizer Original 8oz 70 mL/100mL 57337-0124-01 Ningbo 236 ml — — FDA listed —
Hand Sanitizer with Clip 1.8oz 70 mL/100mL 57337-0125-01 Ningbo 1 bottle — — FDA listed —
Hand Sanitizer 2pk Aloe 2oz 70 mL/100mL 57337-0126-01 Ningbo 1 bottle — — FDA listed —
Hand Sanitizer Aloe 2oz 70 mL/100mL 57337-0127-01 Ningbo 59 ml — — FDA listed —
Hand Sanitizer 2pk Lavender 2oz 70 mL/100mL 57337-0128-01 Ningbo 1 bottle — — FDA listed —
Hand Sanitizer Lavender 2oz 70 mL/100mL 57337-0129-01 Ningbo 59 ml — — FDA listed —
Hand Sanitizer Pouch 70 mL/100mL 57337-0130-01 Ningbo 2.1 ml — — FDA listed —
Hand Sanitizer 24ct Pouch 70 mL/100mL 57337-0131-01 Ningbo 1 pouch — — FDA listed —
Hand Sanitizer Lemon 2oz 70 mL/100mL 57337-0133-01 Ningbo 59 ml — — FDA listed —
Hand Sanitizer Aloe 8oz 70 mL/100mL 57337-0134-01 Ningbo 236 ml — — FDA listed —
Hand sanitizer 8oz with vitamin E 70 mL/100mL 57337-0140-01 REJOICE 236 ml — — FDA listed —
Hand sanitizer 8oz with aloe vera 70 mL/100mL 57337-0141-01 REJOICE 236 ml — — FDA listed —
Hand sanitizer 16.9oz with vitamin E 70 mL/100mL 57337-0142-01 REJOICE 500 ml — — FDA listed —
Ethyl Rubbing Alcohol 70 mL/100mL 59779-0164-43 CVS 473 ml — — FDA listed —
CSI E3 Hand Sanitizer 70 mL/100mL 62654-0139-01 Central 3785 ml — — FDA listed —
DD Mart Hand Sanitizer 70 mL/100mL 63148-0114-08 Apollo 236 ml — — FDA listed —
HiGHMARK 70 mL/100mL 63148-0402-08 Apollo 236 ml — — FDA listed —
Himark 70 mL/100mL 63148-0403-08 Apollo 236 ml — — FDA listed —
Instant Antiseptic Hand Sanitizer 70 mL/100mL 63998-0364-01 United 750 ml — — FDA listed —
Skinsei 700 mg/mL 64942-1740-01 Conopco 118 ml — — FDA listed —
CoreTex Antibacterial Hand Sanitizer 70 mL/100mLthis 65753-0201-01 CoreTex 30 ml — — FDA listed —
Germ Attack Hand Sanitizer .7 mL/mL 66902-0482-02 Natural 59 ml — — FDA listed —
Handy Solutions Hand Sanitizer 70 mL/100mL 67751-0086-01 Navajo 59 ml — — FDA listed —
Alcohol 70 mL/100mL 68196-0602-68 Sam's 2000 ml — — FDA listed —
Zoono Ultra Hand Sanitizer 70 g/100mL 69221-0501-01 Zoono 150 ml — — FDA listed —
Sierra Soft Alcohol Hand Sanitizer 700 mg/mL 70415-0100-01 CWGC 1000 ml — — FDA listed —
Ethyl Rubbing Alcohol 70 mL/100mL 70677-0056-01 STRATEGIC 473 ml — — Discontinued —
Bluesea Instant Hand Sanitizer 70 mL/100mL 72119-0003-01 BLUE 60 ml — — FDA listed —
Ethyl Rubbing Alcohol 70 mL/100mL 72288-0876-43 Amazon.com 473 ml — — FDA listed —
KONIX Alcohol Antiseptic Hand Rub 70 mL/100mL 73107-0105-30 TURKUAZ 30 ml — — FDA listed —
Noshinku Eucalyptus Hand Sanitizer 70 mL/100mL 73898-0002-20 Noshinku 20 ml — — FDA listed —
Noshinku Lavender Hand Sanitizer 70 mL/100mL 73898-0003-20 Noshinku 20 ml — — FDA listed —
Nourishing Hand Sanitizer Orange Coriander 70 mL/100mL 73898-0008-02 Noshinku 3800 ml — — FDA listed —
Hand Sanitizer Vanilla Creme 70 mL/100mL 73898-0009-20 Noshinku 20 ml — — FDA listed —
Hand Sanitizer Pear Blossom Tea 70 mL/100mL 73898-0010-20 Noshinku 20 ml — — FDA listed —
Hand Sanitizer Santal Blanc 70 mL/100mL 73898-0011-20 Noshinku 20 ml — — FDA listed —
Fresh Feels Hand Sanitizer Mist 70 mL/100mL 73905-0045-01 ZHEJIANG 40 ml — — FDA listed —
EcoChoice Sterno Hand Sanitizer Lemon Zest 70 mL/100mL 73926-0753-01 STERNO 2 ml — — FDA listed —
EcoChoice Sterno Hand Sanitizer Clean and Fresh 70 mL/100mL 73926-0754-01 STERNO 59 ml — — FDA listed —
70 Alcohol Hand Sanitizer 70 mL/100mL 74375-0060-01 Iron 355 ml — — FDA listed —
Signature Care Advanced Hand Sanitizer with Aloe 70 mL/100mL 75262-0006-01 ZheJiang 59 ml — — Discontinued —
Instant Hand Sanitizer 70 mL/100mL 75541-0016-01 NINGBO 236 ml — — FDA listed —
Hand sanitizer 8oz with vitamin E 70 mL/100mL 75742-0019-01 Zhejiang 236 ml — — FDA listed —
Hand sanitizer 8oz with aloe vera 70 mL/100mL 75742-0020-01 Zhejiang 236 ml — — FDA listed —
Hand sanitizer 16.9oz with vitamin E 70 mL/100mL 75742-0021-01 Zhejiang 500 ml — — FDA listed —
Hand sanitizer 16.9oz with vitamin E 70 mL/100mL 75742-0029-01 Zhejiang 500 ml — — FDA listed —
Hand sanitizer 8oz with aloe vera 70 mL/100mL 75742-0030-01 Zhejiang 236 ml — — FDA listed —
Hand sanitizer 8oz with vitamin E 70 mL/100mL 75742-0031-01 Zhejiang 236 ml — — FDA listed —
Mellow Hand Sanitizer Aloe 70 mL/100mL 77725-0005-17 L.e.d. 500 ml — — FDA listed —
Ethyl Alcohol 70 mL/100mL 79903-0283-16 Walmart 473 ml — — FDA listed —
DOCTORS TOUCH Hand Sanitizer 70 mL/100mL 80045-0313-00 DOCTOR'S 59 ml — — FDA listed —
b pure Hydrating Hand Sanitizer Vanilla Sugar Cookie Scented 70 mL/100mL 80684-0112-00 FOURSTAR 30 ml — — FDA listed —
b pure Hydrating Hand Sanitizer Frosted Coconut Scented 70 mL/100mL 80684-0113-00 FOURSTAR 30 ml — — FDA listed —
Aloe Scented Hand Sanitizer 70 mL/100mL 80684-0120-00 FOURSTAR 89 ml — — FDA listed —
Eucalyptus Scented Hand Sanitizer 70 mL/100mL 80684-0121-00 FOURSTAR 89 ml — — FDA listed —
Shea Butter Scented Hand Sanitizer 70 mL/100mL 80684-0122-00 FOURSTAR 89 ml — — FDA listed —
B Pure Moisturizing Hand Sanitizer Poppy Scented 70 mL/100mL 80684-0130-00 Fourstar 34 ml — — FDA listed —
B Pure Moisturizing Hand Sanitizer Rainbow Sherbert Scented 70 mL/100mL 80684-0131-00 Fourstar 34 ml — — FDA listed —
B-Pure Moisturizing Hand Sanitizer Honey Crisp Apple Scented 70 mg/100mL 80684-0156-00 FOURSTAR 34 ml — — FDA listed —
B-Pure Moisturizing Hand Sanitizer Pumpkin Vanilla Scented 70 mg/100mL 80684-0157-00 FOURSTAR 34 ml — — FDA listed —
Ethyl Rubbing Alcohol 70 Percent 700 mg/mL 82645-0926-16 Pharma 473 ml — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 83324-0065-02 Chain 59 ml — — FDA listed —
Zoviro 70 mL/100mL 83814-0005-01 Zoviro, 60 ml — — FDA listed —
VQ Hydrating Hand Sanitizer Fresh Watermelon 70 mL/100mL 85980-0001-01 Tychea 30 ml — — FDA listed —
VQ Hydrating Hand Sanitizer Violet Vanilla 70 mL/100mL 85980-0002-01 Tychea 30 ml — — FDA listed —
VQ Hydrating Hand Sanitizer Caramel Pistachio 70 mL/100mL 85980-0003-01 Tychea 1 bottle — — FDA listed —
VQ Hydrating Hand Sanitizer Coconut 70 mL/100mL 85980-0004-01 Tychea 1 bottle — — FDA listed —
VQ Hydrating Hand Sanitizer Pink Dragon Fruit 70 mL/100mL 85980-0005-01 Tychea 1 bottle — — FDA listed —
VQ Hydrating Hand Sanitizer Rose Lychee 70 mL/100mL 85980-0006-01 Tychea 1 bottle — — FDA listed —
VQ Hydrating Hand Sanitizer Sugar Plum 70 mL/100mL 85980-0007-01 Tychea 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

🏛️
2024
On the market since
Jan 2024
📍
2026
Currently FDA-listed
2 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.

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 CZ7BU4QZJZ
    A synthetic organic compound used as a buffer in medicines. It helps maintain the pH (acidity or alkalinity) of liquid formulations to keep the medication stable and suitable for use.
  • UNII 0A5MM307FC
    A synthetic polymer that absorbs water and forms a thick, gel-like substance. In medicines, it works as a thickener and stabilizer to improve texture and help ingredients stay mixed together in creams, gels, and lotions.
  • 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 0RE8K4LNJS
    Isopropyl myristate is an oily liquid made from coconut or palm oil. It's used in medicines as an emollient and penetration enhancer to help the medicine absorb through skin or improve spreadability in topical products.
  • 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 barbadenis leaf juice(aloe vera), amino methylpropanol, carbomer, glycerin, isopropyl myristate, tocopherol acetate (vitamin E acetate), 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.

Manufacturer & labeler

LabelerCoreTex Products Inc
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code65753
First marketedJan 2024
Product typeHuman Otc Drug
Portfolio11 products on file

More NDCs from CoreTex Products Inc labeler code 65753

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.

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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 10 words ▾

Uses: Hand Sanitizer to help reduce bacteria on the skin.

⏱️ Dosage and Administration 17 words ▾

Directions: Put enough product in your palm to cover hands and rub hands together briskly until dry.

⚠️ Warnings 77 words ▾

Warnings: For external use only. Flammable. Do not use near heat, flame or while smoking. When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest. Stop use and ask a doctor if irritation or rash appears and lasts. Keep out of reach of children. If swallowed, get help or contact a Poison Control Center right away.

🧪 Active Ingredient 6 words ▾

Active Ingredients Ethyl Alcohol 70% v/v

🧪 Inactive Ingredients 19 words ▾

Inactive Ingredients: aloe barbadenis leaf juice(aloe vera), amino methylpropanol, carbomer, glycerin, isopropyl myristate, tocopherol acetate (vitamin E acetate), water

🎯 Purpose 2 words ▾

Purpose Antimicrobial

📄 When Using This Product 31 words ▾

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.

📄 Stop Use and Ask a Doctor If 13 words ▾

Stop use and ask a doctor if irritation or rash appears and lasts.

📄 Keep Out of Reach of Children 18 words ▾

Keep out of reach of children. If swallowed, get help or contact a Poison Control Center right away.

📄 Other Information 27 words ▾

Other Information: Store below 104 o F (40 o C), Read the Safety Data Sheet for this Product. You may obtain an SDS from our website: www.coretexproducts.com

📄 Questions or Comments 11 words ▾

Questions and comments: Please call: 1-877-684-5774 or email us at [email protected]

📄 Package Label / Principal Display Panel 28 words ▾

65753-201-01 201-01

65753-201-02 201-02

65753-201-03 201-03

65753-201-05 8oz

65753-201-06 201-06

65753-201-07 201-07

65753-201-10 201-10

65753-201-28 201-28

65753-201-29 201-29

65753-201-30 201-30

65753-201-32 201-32

65753-201-20 and -21 3.75ml

65753-201-35 201-35

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 CoreTex Products Inc. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 13 other package presentations of this same product, including 25 pouches (65753-0201-20), 44 ml (65753-0201-32), 59 ml (65753-0201-02). 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?
CoreTex Products 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.
← 65753-0110-01 · CoreTex 65753-0350-15 · CoreTex →
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.