BODY PRESCRIPTIONS REFRESHING HAND SANITIZER UNSCENTED

Manufacturer
ENCHANTE ACCESSORIES INC. | Xiamen Chengda Industrial Co.,Ltd
Effective date
2020-06-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:15:42

Label at a glance#

ProductBODY PRESCRIPTIONS REFRESHING HAND SANITIZER UNSCENTED
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping For children under 6, use only under adult supervision Not recommended for infants

Storage and handling

Do not store above 105F May discolor some fabrics Harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol Denat. 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

■ To decrease bacteria on the skin that could cause disease
■Recommended for repeated use

WARNINGS

WARNINGS SECTION

For external use only, Hands

Flammable. Keep away from heat and flame

When using this product, keep out of eyes. 
In case of contact with eyes, flush thoroughly with water

Avoid contact with broken skin

Do not inhale or ingest

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation develops

keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a poison control center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping

For children under 6, use only under adult supervision

Not recommended for infants

Other information

STORAGE AND HANDLING SECTION

Do not store above 105F

May discolor some fabrics

Harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, PEG-40 Hydrogenated castor oil, Carbomer, Triethanolamine, Blue 1, Red 33

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

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
50563-197-012022-01-28C16284748780-1d6a99b39-59cd-a426-e053-dadaa90af4c2d5c5b0ed-0cd1-4cf0-9db7-818999551afe

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50563-197-01BODY PRESCRIPTIONS REFRESHING HAND SANITIZER UNSCENTED236 mL in 1 BOTTLEGEL2361

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50563-197BODY PRESCRIPTIONS REFRESHING HAND SANITIZER UNSCENTED (ETHYL ALCOHOL) GEL [ENCHANTE ACCESSORIES INC.]1Legacy NDC, 1 package rows20200602_d5c5b0ed-0cd1-4cf0-9db7-818999551afe.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50563-19750563-197-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
a70e30dd-8798-0a16-e053-2a95a90abde3d5c5b0ed-0cd1-4cf0-9db7-818999551afe2020-06-01WarningsExact identifier
spl id: a70e30dd-8798-0a16-e053-2a95a90abde3
spl set id: d5c5b0ed-0cd1-4cf0-9db7-818999551afe

Reported adverse events (FAERS/openFDA)#

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