HAND SANITIZER FRAGRANCE FREE- ethyl alcohol solution

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Interline Brands, Inc, Vi-Jon, LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Uses

To decrease bacteria on the skin that could cause disease

Recommended for repeated use

Warnings

FLAMMABLE, keep away from fire and flame

For external use only

When using this product

do not use in or near eyes   

Stop use and ask a doctor

if irritation or redness develops.  If condition persists for more than 72 hours consult a doctor.

Keep out of reach of children.

If swallowed, seek immediate medical attention or call a poison control center.

Directions

Wet hands thoroughly with product and allow to dry without wiping.

Inactive ingredients

Water, Isopropyl Alcohol, PEG-12 Dimethicone, Glycerin, Caprylic/Capric Triglyceride, Isopropyl Myristate

Additional rear label text for manual dispensers

Renown Image Manual Sanitzer Refill

Fragrance Free OMSID 313656114

NSF

Nonfood Compounds

Program Listed E3

Distributed exclusively by: Home Depot Pro

701 San Marco Blvd. Jacksonville, FL 32207

alcohol permit SDA-MO-15036

DSP-MO-28, DSP-MO-34

Additional rear label text for automatic dispensers

Renown Image Automated Sanitzer Refill

Fragrance Free OMSID 313656113

NSF

Nonfood Compounds

Program Listed E3

Distributed exclusively by: Home Depot Pro

701 San Marco Blvd.  Jacksonville, FL 32207

alcohol permit SDA-MO-15036

DSP-MO-28, DSP-MO-34

principal display panel

Renown Image

Manual Sanitizer Refill

Fragrance Free

1,000 mL (33.8 FL OZ)

OMSID 313656114

principal display panel

Renown Image

Automated Sanitizer Refill

Fragrance Free

1,000 mL (33.8 FL OZ)

OMSID 313656113

INGREDIENTS AND APPEARANCE

HAND SANITIZER   FRAGRANCE FREE
ethyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71896-701
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PEG-12 DIMETHICONE (UNII: ZEL54N6W95)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71896-701-86	1000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	10/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/02/2016

Labeler - Interline Brands, Inc (080792989)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(71896-701)