MAGIC XTREME XTRA HAND SANITIZER

Manufacturer
ENSOBRETADOS Y DERIVADOS S.A. DE C.V.
Effective date
2021-01-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:37:11

Label at a glance#

ProductMAGIC XTREME XTRA HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer to decrease bacteria on the skin.

Dosage and administration

■ Wet hands thoroughly. Allow to dry without wiping. ■ Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

■ Store between 15-30C (59-86F) ■ Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 72%

PURPOSE

OTC - PURPOSE SECTION

Antibacterial

USES

INDICATIONS & USAGE SECTION

Hand sanitizer to decrease bacteria on the skin.

WARNINGS

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

■ in children less than 2 months of age

■ on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

■ Wet hands thoroughly. Allow to dry without wiping.

■ Supervise children under 6 years of age when using this product to avoid swallowing.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

■ Store between 15-30C (59-86F)

■ Avoid freezing and excessive heat above 40C (104F)

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Carbopol, Glycerin, Triethanolamine, Water (Aqua).

QUESTIONS OR COMMENTS?

OTC - QUESTIONS SECTION

1-855-349-7735 or visit www.eydmx.com

MAGIC XTREME XTRA HAND SANITIZER 2 mL (NDC 78885-002-00)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Magic Xtreme Hand Sanitizer 2 mLMagic Xtreme Hand Sanitizer 2 mL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2277550ethanol 72 % Topical GelPSN1
2277550ethanol 0.72 ML/ML Topical GelSCD1
2277550ethanol 72 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78885-002-002022-07-29C16284748780-1e4f33bdf-a065-d8a0-e053-dadaa90a6e4eMAGIC XTREME XTRA HAND SANITIZER 2 mL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78885-002-00MAGIC XTREME XTRA HAND SANITIZER2 mL in 1 BOTTLE, PLASTICGEL21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78885-002MAGIC XTREME XTRA HAND SANITIZER (ETHYL ALCOHOL) GEL [ENSOBRETADOS Y DERIVADOS S.A. DE C.V.]1Legacy NDC, 1 package rows20210122_b96395f9-b259-7e56-e053-2a95a90a8c80.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78885-00278885-002-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
b96395f9-b25a-7e56-e053-2a95a90a8c80b96395f9-b259-7e56-e053-2a95a90a8c802021-01-15WarningsExact identifier
spl id: b96395f9-b25a-7e56-e053-2a95a90a8c80
spl set id: b96395f9-b259-7e56-e053-2a95a90a8c80

Reported adverse events (FAERS/openFDA)#

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