VANILLA SCENT HAND SANITIZER GEL

Manufacturer
Amber Glow Cosmetics Limited
Effective date
2026-06-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-06-11 05:11:18

Label at a glance#

ProductVANILLA SCENT HAND SANITIZER
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

• Apply 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

• Apply 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, Acrylates/ C10-30 Alkyl Acrylate Crosspolymer, Fragrance, Tetrahydroxypropyl Ethylenediamine, Polyethylene Terephthalate. 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: Amber Glow Cosmetics Limited
Unit 1806, 18/F., 9 Wing Hong Street,
Cheung Sha Wan, Hong Kong
Questions or Comments call (877) 711-8333
Made in China

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VANILLA SCENT HAND SANITIZERVANILLA SCENT HAND SANITIZER

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130810208306749GTIN-13: 0810208306749
EAN-13: 0810208306749
GTIN-12: 810208306749
UPC-A: 810208306749
GTIN storage (14 digits): 00810208306749
87302214-2.jpg

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87302-21487302-214-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
VANILLA SCENT HAND SANITIZERETHYL ALCOHOLAmber Glow Cosmetics Limited67c2cb48-481d-41aa-a11d-e00d81d7a34a2026-06-05WarningsExact identifier
ndc (package): 87302-214-14
ndc (product): 87302-214
ndc11 (package): 87302021414
spl id: c454f2f5-245e-4108-ace2-02e88755eac9
spl set id: 67c2cb48-481d-41aa-a11d-e00d81d7a34a

Reported adverse events (FAERS/openFDA)#

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