Air and Water

Manufacturer
Pearl World Inc.
Effective date
2020-09-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:29:59

Label at a glance#

ProductAir and Water Hand Sanitizer - Merry Peppermint
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

• To decrease bacteria on the skin that could cause disease. • When water, soap and towel are not available. • Recommended for repeated use.

Storage and handling

Other informatio n • Store below 105°F (40°C). • May discolor certain fabrics. • Harmful to wood finishes & plastics.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• To decrease bacteria on the skin that could cause disease. • When water, soap and towel are not available. • Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only: hands.

Flammable. Keep away from fire or flame.

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

Stop use and ask a doctor if • Redness or irritation develop • Condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. • Children should be supervised by an adult when using this product. • If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions • Wet hands thoroughly with product and allow to dry without wiping. • No rinsing required. • For children under 6, use only under adult supervision. • Not recommended for infants.

STORAGE AND HANDLING SECTION

Other information • Store below 105°F (40°C). • May discolor certain fabrics. • Harmful to wood finishes & plastics.

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water (Aqua), Triethanolamine, Carbomer, Aloe Barbadensis Leaf Extract, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E). Main Contain: FD & C Red 40 (CI 16035), FD & C Yellow 6 (CI 15985), FD & C Violet 2 (CI 60725), FD & C Blue 1 (CI 42090), FD & C Yellow 5 (CI 19140), FD & C Red 33(CI 17200).

SPL UNCLASSIFIED SECTION

70% Alcohol

Manufactured for and distributed by Pearl world Inc, NY, NY 10019
Pearlworldinc.com All rights reserved. Designed in the USA. Made in PRC.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69933-400-502022-01-28C16284748780-1d6a99b39-e2d9-a426-e053-dadaa90af4c2AIR&WATER Merry Peppermint Hand Sanitizer
69933-400-602022-01-28C16284748780-1d6a99b39-e2d9-a426-e053-dadaa90af4c2AIR&WATER Merry Peppermint Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69933-400-50Air and WaterHand Sanitizer - Merry Peppermint500 mL in 1 BOTTLE, PUMPGEL5001
69933-400-60Air and WaterHand Sanitizer - Merry Peppermint60 mL in 1 BOTTLEGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69933-400AIR AND WATER HAND SANITIZER - MERRY PEPPERMINT (ETHYL ALCOHOL) GEL [PEARL WORLD INC.]1Legacy NDC, 2 package rows20200924_019a55c4-0584-4d32-8f85-0af6b0ca943c.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69933-40069933-400-50, 69933-400-60

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
fd820ecb-bb3e-4f6b-8156-0c630bef49a3019a55c4-0584-4d32-8f85-0af6b0ca943c2020-09-17WarningsExact identifier
spl id: fd820ecb-bb3e-4f6b-8156-0c630bef49a3
spl set id: 019a55c4-0584-4d32-8f85-0af6b0ca943c

Reported adverse events (FAERS/openFDA)#

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