IDLIFE SANITIZE MOISTURIZING HAND SANITIZER- benzalkonium chloride lotion

IDLife SANITIZE MOISTURIZING HAND SANITIZER by

Drug Labeling and Warnings

IDLife SANITIZE MOISTURIZING HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Willspeed Technologies LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

DRUG FACTS

Active Ingredient

Benzalkonium chloride 0.13%

Purpose

Antiseptic

Uses

Kills 99.99 % germs and moisturizes skin.

Warnings

For external use only.

Do not use in the eyes.

In case of eye contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

if irritation or redness develops, or if condition persists more than 72 hours.

Keep out of reach of children.

Instruct children on proper use. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply a small amount to hands and rub until dry. Lotion does not replace soap and water.

Inactive Ingredients

Aloe Barbadensis Extract, Avena Sativa (Oat) Extract, Behentrimonium Methosulfate, Caprylyl Glycol, Cetearyl Alcohol, Cetrimonium Chloride, Dimethicone, Glycerin, Hydrolyzed Soy Protein, Mentha Piperita (Peppermint) Essential Oil, Phenoxyethanol, Polysorbate 60, Simmondsia Chinensis (Jojoba) Seed Oil, Tetrasodium EDTA, Vitamin A Palmitate, Vitamin E Acetate, Water.

PRINCIPAL DISPLAY PANEL

IDLife

SANITIZE+
MOISTURIZING HAND SANITIZER
Kills 99.9% OF GERMS PROTECTION UP TO 4 HOURS
2 fl. oz. (59mL)

PATENTED FORMULA

INGREDIENTS AND APPEARANCE

IDLIFE SANITIZE MOISTURIZING HAND SANITIZER 
benzalkonium chloride lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69243-1111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0013 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AVENA SATIVA LEAF (UNII: 206PI19V7R)
BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCERIN (UNII: PDC6A3C0OX)
SOY PROTEIN (UNII: R44IWB3RN5)
PEPPERMINT OIL (UNII: AV092KU4JH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
JOJOBA OIL (UNII: 724GKU717M)
SORBIC ACID (UNII: X045WJ989B)
EDETATE SODIUM (UNII: MP1J8420LU)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69243-1111-1	30 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/24/2020
2	NDC: 69243-1111-2	44 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/24/2020
3	NDC: 69243-1111-3	59 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/24/2020
4	NDC: 69243-1111-4	118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/24/2020
5	NDC: 69243-1111-5	237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/24/2020

Labeler - Willspeed Technologies LLC (019063540)