FDA.reportPublic FDA data

QYK Brands

Manufacturer
Guangzhou C-kang Biotechnology Co., Ltd.
Effective date
2020-07-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:00

Label at a glance#

ProductQYK Brands
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Other information • Store below 110°F (43°C) • May discolor some fabrics.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Uses: • Hand Sanitizer to help decrease bacteria on the skin that could cause disease. • Recommended for repeated use.

WARNINGS SECTION

Warnings For external use only, use on hands only.

Flammable. Keep away from fire or flame.

When using this product: • Avoid contact with eyes. In case of contact with eyes, flush thoroughly with water. • Avoid contact with broken skin. • Do not inhale or ingest.

Stop use and ask doctor if • Irritation and redness develops. • Condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions • Pump as needed into your palms and thoroughly spread on both hands. Rub into skin until dry. • For children under 6, use only under adult supervision. • Not recommended for infants.

STORAGE AND HANDLING SECTION

Other information • Store below 110°F (43°C) • May discolor some fabrics.

INACTIVE INGREDIENT SECTION

Inactive ingredients Water, Glycerin, Aloe vera, Carbomer, Polyacrylate crosspolymer, Fragrance

SPL UNCLASSIFIED SECTION

ALOE VERA REFRESHING GEL

Kills More Than 99.99% of Germs and Bacteria

Distributed By:

QYK BRANDS, LLC.

Garden Grove, CA 92843

www.DrJsNatural.com

Questions or Comments

Please Call: 1-888-308-7078

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackagingPackagingPackagingPackagingPackagingPackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74416-171-022022-01-28C16284748780-1d6a99b39-ab8a-a426-e053-dadaa90af4c2Dr. J's™ Natural ADVANCED FORMULA HAND SANITIZER
74416-171-032022-01-28C16284748780-1d6a99b39-ab8a-a426-e053-dadaa90af4c2Dr. J's™ Natural ADVANCED FORMULA HAND SANITIZER
74416-171-042022-01-28C16284748780-1d6a99b39-ab8a-a426-e053-dadaa90af4c2Dr. J's™ Natural ADVANCED FORMULA HAND SANITIZER
74416-171-082022-01-28C16284748780-1d6a99b39-ab8a-a426-e053-dadaa90af4c2Dr. J's™ Natural ADVANCED FORMULA HAND SANITIZER
74416-171-102022-01-28C16284748780-1d6a99b39-ab8a-a426-e053-dadaa90af4c2Dr. J's™ Natural ADVANCED FORMULA HAND SANITIZER
74416-171-162022-01-28C16284748780-1d6a99b39-ab8a-a426-e053-dadaa90af4c2Dr. J's™ Natural ADVANCED FORMULA HAND SANITIZER
74416-171-352022-01-28C16284748780-1d6a99b39-ab8a-a426-e053-dadaa90af4c2Dr. J's™ Natural ADVANCED FORMULA HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74416-171-02QYK Brands60 mL in 1 BOTTLEGEL601
74416-171-03QYK Brands100 mL in 1 BOTTLEGEL1001
74416-171-04QYK Brands120 mL in 1 BOTTLEGEL1201
74416-171-08QYK Brands240 mL in 1 BOTTLEGEL2401
74416-171-10QYK Brands300 mL in 1 BOTTLEGEL3001
74416-171-16QYK Brands500 mL in 1 BOTTLEGEL5001
74416-171-35QYK Brands1000 mL in 1 BOTTLEGEL10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74416-171QYK BRANDS (ETHYL ALCOHOL) GEL [GUANGZHOU C-KANG BIOTECHNOLOGY CO., LTD.]1Legacy NDC, 7 package rows20200711_bdfe9ead-1615-4962-bed7-7c8c14f31038.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74416-17174416-171-02, 74416-171-03, 74416-171-04, 74416-171-08, 74416-171-10, 74416-171-16, 74416-171-35

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
AMMONIUM ACRYLOYL DIMETHYLTAURATE/METHACRYLATE, DIMETHYLACRYLAMIDE AND METHACRYLIC ACID COPOLYMER, PPG-3 GLYCERYL TRIACRYLATE CROSSLINKED (100000 MW)WR7H9IW2XXIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
b0bef386-1ced-464d-8f87-0b46520a9dd2bdfe9ead-1615-4962-bed7-7c8c14f310382020-07-01WarningsExact identifier
spl id: b0bef386-1ced-464d-8f87-0b46520a9dd2
spl set id: bdfe9ead-1615-4962-bed7-7c8c14f31038

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.