FDA.reportPublic FDA data

Dr Lift Antibacterial Hand Sanitizer

Manufacturer
Spa de Soleil
Effective date
2025-11-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:43:38

Key Label Information#

Active Ingredients And Purpose

Active Ingredient

Ethyl Alcohol 70.0 %

Purpose

Antimicrobial

Uses

Directions

Place enough product in the palm of your hands to thoroughly cover your hands. Rub hands together briskly until product is completely absorbed and hands are dry.

Warnings

Warnings

Warnings Flammable. Keep away from fire or flame. For external use only. When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions And Dosage

Directions

Place enough product in the palm of your hands to thoroughly cover your hands. Rub hands together briskly until product is completely absorbed and hands are dry.

Other Label Information

Inactive Ingredients

Inactive Ingredients: Aqua, Glycerin, *CO Glycerin, *CO Humulus Lupulus (Hops) Extract, *CO Lavandula Angustifolia (Lavender) Flower/Leaf/Stem Extract, *CO Calendula Officinalis Flower Extract, *CO Chamomilla Recutita (Matricaria) Flower Extract, *CO Citrus Limon (Lemon) Peel Extract, *CO Cucumis Sativus (Cucumber) Seed Extract, *CO Camellia Sinensis Leaf Extract, *CO Pyrus Malus (Apple) Fruit Extract, *CO Spirulina Platensis Extract, Xanthan Gum. *CO Certified Organic

Label Images#

EnglishAntibacterialHandSanitizer
EnglishAntibacterialHandSanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN3
581662ethanol 0.7 ML/ML Topical GelSCD3
581662ethanol 70 % Topical GelSY3
581662ethyl alcohol 70 % Topical GelSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68062-2250-1Dr Lift Antibacterial Hand Sanitizer240 mL in 1 BOTTLE, PUMPGEL2403

Products#

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68062-225068062-2250-1

Ingredients#

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
XANTHAN GUMTTV12P4NEEIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT

Complete SPL Sections#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70.0 %

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Warnings

WARNINGS SECTION

Warnings Flammable. Keep away from fire or flame. For external use only. When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

INDICATIONS & USAGE SECTION

Place enough product in the palm of your hands to thoroughly cover your hands. Rub hands together briskly until product is completely absorbed and hands are dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Aqua, Glycerin, *CO Glycerin, *CO Humulus Lupulus (Hops) Extract, *CO Lavandula Angustifolia (Lavender) Flower/Leaf/Stem Extract, *CO Calendula Officinalis Flower Extract, *CO Chamomilla Recutita (Matricaria) Flower Extract, *CO Citrus Limon (Lemon) Peel Extract, *CO Cucumis Sativus (Cucumber) Seed Extract, *CO Camellia Sinensis Leaf Extract, *CO Pyrus Malus (Apple) Fruit Extract, *CO Spirulina Platensis Extract, Xanthan Gum. *CO Certified Organic

Source Document#

Source XML