Hand Savior Radiance Boosting Serum

Manufacturer
Bell International Laboratories, Inc
Effective date
2023-09-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:26:27

Label at a glance#

ProductHand Savior Radiance Boosting Serum
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together to dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 60% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only

Flammable. Keep away from heat or flame

Do not use

  • on children less than 2 months of age
  • on open skin wounds

When using this product keep out of eyes, ears, and mouth. if case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These man be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together to dry.

Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

OTHER SAFETY INFORMATION

Store between 15-30 C (59-86 F)

Avoid freezing and excessive heat above 40 C (104F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Niacinamide, Vitis Vinifera (Grape) Seed Oil, Carthanum Tinctorius (Safflower) Oleosomes, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Hydroxyethylcellulose, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Citrus Aurantium Dulcis (Orange) Flower OIl, CItrus Nobilis (Mandarin Orange) Peel Oil, Sodium Hyaluronate, Gluconolactone, Citrus Aurantium Dulcis (Orange) Peel Oil, Sodium Benzoate, Sodium Hydroxide, Dec-9-en-2-one, Dimethylhydroxy Furanone, Ethyl 2-Methybutyrate, Ethyl Cinnamate, Ethyl Lactate, Ethyl Propionate, Hexenyl Acetone, Ionone, Isoamyl Acetate, Methoxyphenybutanone, Triethyl Citrate, Vanillin, Benzyl Acetate, Ethy Acetate.

Questions?

OTC - QUESTIONS SECTION

(888)7001-9899

Serious side effects associated with use of this product may be reported to this number.

primary package label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

primary labelprimary label

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76150-27176150-271-34

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
04b92c08-1092-3f9a-e063-6394a90a0be5bba01ed5-739e-1233-e053-2a95a90aa45f2023-09-06WarningsExact identifier
spl id: 04b92c08-1092-3f9a-e063-6394a90a0be5
spl set id: bba01ed5-739e-1233-e053-2a95a90aa45f

Reported adverse events (FAERS/openFDA)#

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