Holiday CANDY Hand Sanitizer

Manufacturer
BBC GROUP LIMITED
Effective date
2019-04-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:25:12

Label at a glance#

ProductHoliday CANDY Hand Sanitizer
Label structure10 sections

Indications and uses

To reduce bacteria on skin

Dosage and administration

Apply dime sized amount to hands and rub until dry. Supervise children under 6 years of age.

Label contents#

Full prescribing information#

Active ingredient Purpose

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%...........Antibacterial

Uses

INDICATIONS & USAGE SECTION

To reduce bacteria on skin

Warnings

WARNINGS SECTION

For external use only

Flammable, keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product avoid contact with eye. If contact with occurs,flush eyes with water.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears that lasts.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply dime sized amount to hands and rub until dry.

Supervise children under 6 years of age.

OTHER SAFETY INFORMATION

Do not store above 105'F

May discolor certain fabrics or surfaces.

INACTIVE INGREDIENT SECTION

Water, fragrance, PEG-40 Hydrogenated Castor Oil, Acylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Blue No.1(CI 42090), Yellow 5(CI 19140).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

76383-01176383-011

Products#

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DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76383-01176383-011-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MINGR

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
8765423b-c53c-07d8-e053-2995a90a4cde87655c3e-acb2-bdc2-e053-2a95a90ae2a12019-04-26WarningsExact identifier
spl id: 8765423b-c53c-07d8-e053-2995a90a4cde
spl set id: 87655c3e-acb2-bdc2-e053-2a95a90ae2a1

Reported adverse events (FAERS/openFDA)#

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