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NDC 69243-1111-01 IDLife SANITIZE MOISTURIZING HAND SANITIZER 0.0013 g/mL Details

IDLife SANITIZE MOISTURIZING HAND SANITIZER 0.0013 g/mL

IDLife SANITIZE MOISTURIZING HAND SANITIZER is a TOPICAL LOTION in the HUMAN OTC DRUG category. It is labeled and distributed by Willspeed Technologies LLC. The primary component is BENZALKONIUM CHLORIDE.

Product Information

NDC	69243-1111
Product ID	69243-1111_ce537db5-479a-4dcb-a3b0-55b53ac26273
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	IDLife SANITIZE MOISTURIZING HAND SANITIZER
Proprietary Name Suffix	n/a
Non-Proprietary Name	Benzalkonium Chloride
Product Type	HUMAN OTC DRUG
Dosage Form	LOTION
Route	TOPICAL
Active Ingredient Strength	0.0013
Active Ingredient Units	g/mL
Substance Name	BENZALKONIUM CHLORIDE
Labeler Name	Willspeed Technologies LLC
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part333A
Listing Certified Through	2023-12-31

Package

Package Images

NDC 69243-1111-01 (69243111101)

Pricing Information	N/A
NDC Package Code	69243-1111-1
Billing NDC	69243111101
Package	30 mL in 1 BOTTLE, PUMP (69243-1111-1)
Marketing Start Date	2020-11-24
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL e20dfe84-49a2-4a42-a0ac-995bd3268833 Details

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

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

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date
Packaging
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 Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	11/24/2020

Labeler - Willspeed Technologies LLC (019063540)

Revised: 1/2022

Document Id: ce537db5-479a-4dcb-a3b0-55b53ac26273

Set id: e20dfe84-49a2-4a42-a0ac-995bd3268833

Version: 2

Effective Time: 20220114