Janitex

Janitex
SPL v1
SPL
SPL Set ID ba3f957d-b477-4c51-8213-b67bb7c00ab3
Route
TOPICAL
Published
Effective Date 2020-08-13
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Benzalkonium (0.1 g)
Inactive Ingredients
Water Phenoxyethanol Propylene Glycol Cocamidopropyl Betaine Polyoxyl 40 Hydrogenated Castor Oil Benzoic Acid Edetate Sodium Dehydroacetic Acid Sodium Hydroxide

Identifiers & Packaging

Marketing Status
OTC MONOGRAPH NOT FINAL Active Since 2020-08-11

Description

Benzalkonium Chloride (0.1%)

Purpose

Antiseptic


Medication Information

Purpose

Antiseptic

Description

Benzalkonium Chloride (0.1%)

Uses
  • To decrease bacteria on the skin that could cause disease
Section 42229-5

pH 5.5

E Vitamin

DERMATOLOGICALLY TESTED 

+ moisturizer 

non-woven fabric

Bleach Free

Ultra Protection

ANTIBACTERIAL

Distributed by Pacific Health Systems Inc.

19 Commerce Road Unit E Fairfield, NJ 07004

[email protected] www.janitexus.com

Section 50565-1
  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Warnings
  • For external use only, harmful if swallowed.
  • Do not use as baby wipe.
  • Do not flush.
  • Do not use on open skin wounds.
  • 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 allergic reaction occurs.
  • Flammable - Keep away from fire or flame

Packaging

Directions

• Open lid, gently peel back resealable label, remove and use wipes as required. Keep lid closed to prevent moisture loss.

• No need to rinse after usage. Allow skin to dry without wiping. • For adults and children 2 years and over. Discard properly after use. • Supervise children under 6 years of age when using this product to avoid swallowing.

Drug Facts

Other Information
  • Store in dry and cool place and away from oxidizers.
Active Ingredients

Benzalkonium Chloride (0.1%)

Inactive Ingredients

Aqua, Phenoxyethanol, Propylene Glycol, Parfum, Cocamidopropyl Betaine, PEG-40 Hydrogenated Castor Oil, Benzoic Acid, Tetrasodium EDTA, Dehydroacetic Acid, Sodium Hydroxide


Structured Label Content

Uses
  • To decrease bacteria on the skin that could cause disease
Section 42229-5 (42229-5)

pH 5.5

E Vitamin

DERMATOLOGICALLY TESTED 

+ moisturizer 

non-woven fabric

Bleach Free

Ultra Protection

ANTIBACTERIAL

Distributed by Pacific Health Systems Inc.

19 Commerce Road Unit E Fairfield, NJ 07004

[email protected] www.janitexus.com

Section 50565-1 (50565-1)
  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Purpose

Antiseptic

Warnings
  • For external use only, harmful if swallowed.
  • Do not use as baby wipe.
  • Do not flush.
  • Do not use on open skin wounds.
  • 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 allergic reaction occurs.
  • Flammable - Keep away from fire or flame

Packaging

Directions

• Open lid, gently peel back resealable label, remove and use wipes as required. Keep lid closed to prevent moisture loss.

• No need to rinse after usage. Allow skin to dry without wiping. • For adults and children 2 years and over. Discard properly after use. • Supervise children under 6 years of age when using this product to avoid swallowing.

Drug Facts

Other Information
  • Store in dry and cool place and away from oxidizers.
Active Ingredients

Benzalkonium Chloride (0.1%)

Inactive Ingredients (Inactive ingredients)

Aqua, Phenoxyethanol, Propylene Glycol, Parfum, Cocamidopropyl Betaine, PEG-40 Hydrogenated Castor Oil, Benzoic Acid, Tetrasodium EDTA, Dehydroacetic Acid, Sodium Hydroxide


Advanced Ingredient Data


Raw Label Data

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