SANITIZE ASAP HAND SANITIZER

Manufacturer
New World Holdings, Inc.
Effective date
2020-05-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:11:11

Label at a glance#

ProductSANITIZE ASAP HAND SANITIZER
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

Active ingredient:

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol Denatured.................80%

Purpose:

OTC - PURPOSE SECTION

Anti-bacterial

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Glycerin, Hydrogen Peroxide, Distilled Water

INDICATIONS & USAGE SECTION

Uses: to decrease bacteria on the skin that could interfere with good health, recommended for repeated use.

DOSAGE & ADMINISTRATION SECTION

Directions: wet the hands thoroughly with the product and rub hands until dry.

WARNINGS SECTION

keep out of the eyes, avoid contact with broken skin, if swallowed get medical help or contact a poison control center.

Flammable, keep away from heat and flame.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

SPL UNCLASSIFIED SECTION

ANTI-BACTERIAL

KILLS BACTERIA!

MADE IN USA

LABORATORY CRAFTED - ANTI-BACTERIAL BLEND

FROM THE RESEARCH LABORATORIES OF NWH-USA

BE SAFE

BE CAUTIOUS

These statements have not been evaluated by the Food and Drug Administration.

This product is not intended to diagnose, treat cure or prevent any disease.

SANITIZEASAP.COM

New World Cosmetics and Medicinals.
1080 Holland Drive. Suite 1,
Boca Raton, Florida 33487

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN1
1039339ethanol 0.8 ML/ML Topical SolutionSCD1
1039339ethanol 80 % Topical SolutionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73871-202-082022-01-28C16284748780-1d6a99b39-8c7d-a426-e053-dadaa90af4c2SANITIZE ASAP HAND SANITIZER
73871-202-162022-01-28C16284748780-1d6a99b39-8c7d-a426-e053-dadaa90af4c2SANITIZE ASAP HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73871-202-08SANITIZE ASAP HAND SANITIZER236 mL in 1 BOTTLELIQUID2361
73871-202-16SANITIZE ASAP HAND SANITIZER473 mL in 1 BOTTLELIQUID4731

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73871-202SANITIZE ASAP HAND SANITIZER (ETHYL ALCOHOL) LIQUID [NEW WORLD HOLDINGS, INC.]1Legacy NDC, 2 package rows20200514_68b5eebf-06ea-45f3-83e4-d712028f0808.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73871-20273871-202-08, 73871-202-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML · Source PDF

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
8a3b9bfd-020c-4864-91ee-92c0daf903d668b5eebf-06ea-45f3-83e4-d712028f08082020-05-04WarningsExact identifier
spl id: 8a3b9bfd-020c-4864-91ee-92c0daf903d6
spl set id: 68b5eebf-06ea-45f3-83e4-d712028f0808

Reported adverse events (FAERS/openFDA)#

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