HAND SANITIZER SUGAR VANILLA

Manufacturer
Pearl World Inc.
Effective date
2025-10-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:43:41

Label at a glance#

ProductHAND SANITIZER SUGAR VANILLA
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

Dosage and administration

• Spray product in your palm and rub hands together until dry. • For children under 6, use only under adult supervision. • Not recommended for infants.

Storage and handling

• Do not store above 105°F. • May discolor some fabrics. • Harmful to wood finishes and 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. 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.

Directions

DOSAGE & ADMINISTRATION SECTION

• Spray product in your palm and rub hands together until dry.
• For children under 6, use only under adult supervision.
• Not recommended for infants.

Other Information

STORAGE AND HANDLING SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Dipropylene Glycol, Glycereth-26, Fragrance, Butylene Glycol, Leuconostoc/Radish Root Ferment Filtrate, Aloe Barbadensis Leaf Juice, Phenoxyethanol. May Contain: Red 40 Lake (CI 16035), Red 33 Lake (CI 17200), Red 4 Lake (CI 14700), Yellow 5 Lake (CI 19140:1), Blue 1 Lake (CI 42090:2).

SPL UNCLASSIFIED SECTION

Distributed By: Pearl World Inc.
152 W 57th St, Fl 48. NY, NY 10019
Questions or Comments call (877) 711-8333
Made in China

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HAND SANITIZER SUGAR VANILLAHAND SANITIZER SUGAR VANILLA

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041849ethanol 70 % Topical SprayPSN1
1041849ethanol 0.7 ML/ML Topical SpraySCD1
1041849ethanol 70 % Topical SpraySY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69933-125-05HAND SANITIZER SUGAR VANILLA1 in 1 POUCHSPRAY11
69933-125-05HAND SANITIZER SUGAR VANILLA40 mL in 1 BOTTLE, SPRAYSPRAY401

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
69933-12569933-125-05

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
HAND SANITIZER SUGAR VANILLAETHYL ALCOHOLPearl World Inc.d29b8d41-acae-41f5-9d2c-9c06e3c166282025-10-06WarningsExact identifier
ndc (package): 69933-125-05
ndc (product): 69933-125
ndc11 (package): 69933012505
spl id: 186d589c-4e71-4828-8fcd-d2f680d7e228
spl set id: d29b8d41-acae-41f5-9d2c-9c06e3c16628

Reported adverse events (FAERS/openFDA)#

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