ZAP Hand Sanitizer

Manufacturer
Beverly Pharmacy, Inc. Dba Zap Hand Sanitizer
Effective date
2020-08-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:26:09

Label at a glance#

ProductZAP Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

hand sanitizer to decrease bacteria on the skin recommended for repeated use for use when soap and water are not available

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping supervise children under 6 years of age when using this product to avoid swallowing

Storage and handling

store between 15-30°C (59-86°F) avoid freezing and excessive heat above 40°C (104°F)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to decrease bacteria on the skin
  • recommended for repeated use
  • for use when soap and water are not available

Warnings

WARNINGS SECTION

Flammable, keep away from fire/flame

For external use only

Do not use

• in children less than 2 months of age

• on open skin wounds

When using this product • do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if

• irritation and redness develop

• condition persists for more than 72 hours

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 with product and 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 15-30°C (59-86°F)
  • avoid freezing and excessive heat above 40°C (104°F)

INACTIVE INGREDIENT SECTION

Inactive ingredients   aloe vera, vitamin E

Questions? +1-310-499-3342

OTC - QUESTIONS SECTION

You may also report serious side effects to this phone number. Mon-Fri 9:00 AM - 5:00 PM

SPL UNCLASSIFIED SECTION

ANTISEPTIC HAND SANITIZER

Manufactured for: Beverly Pharmacy Inc, dba ZAP Hand Sanitizer, PO Box 3007, BH, CA 90212

COUNTRY OF ORIGIN: CHINA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

untitleduntitled

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN1
1047755ethanol 0.75 ML/ML Topical SolutionSCD1
1047755ethanol 75 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
90041-800-02ZAP Hand Sanitizer59 mL in 1 TUBELIQUID591
90041-800-04ZAP Hand Sanitizer118 mL in 1 TUBELIQUID1181
90041-800-08ZAP Hand Sanitizer236 mL in 1 BOTTLELIQUID2361
90041-800-16ZAP Hand Sanitizer473 mL in 1 BOTTLELIQUID4731
90041-800-32ZAP Hand Sanitizer946 mL in 1 BOTTLELIQUID9461
90041-800-64ZAP Hand Sanitizer1893 mL in 1 BOTTLELIQUID18931
90041-800-99ZAP Hand Sanitizer3785 mL in 1 BOTTLELIQUID37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
90041-800ZAP HAND SANITIZER (ETHYL ALCOHOL) LIQUID [BEVERLY PHARMACY, INC. DBA ZAP HAND SANITIZER]1Legacy NDC, 7 package rows20200829_59a50110-89db-47f4-b626-dcb2b91f6ae6.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90041-80090041-800-02, 90041-800-04, 90041-800-08, 90041-800-16, 90041-800-32, 90041-800-64, 90041-800-99

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT

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
2da38781-a469-4f54-926f-40e75ca960e659a50110-89db-47f4-b626-dcb2b91f6ae62020-08-19WarningsExact identifier
spl id: 2da38781-a469-4f54-926f-40e75ca960e6
spl set id: 59a50110-89db-47f4-b626-dcb2b91f6ae6

Reported adverse events (FAERS/openFDA)#

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