cwgc (as pld) - puro non-alcohol foam hand sanitizer (70415-405)

cwgc (as pld) - puro non-alcohol foam hand sanitizer (70415-405)
SPL v6
SPL
SPL Set ID 437de694-03eb-495a-a4b3-ff5c69bcb0ec
Route
topical
Published
Effective Date 2017-08-04
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
benzalkonium (0.13 g)
Inactive Ingredients
water coco glucoside laurtrimonium chloride cocamidopropylamine oxide anhydrous citric acid

Identifiers & Packaging

Marketing Status
otc monograph drug active Since 2017-03-22

Purpose

Antibacterial

Description

BENZALKONIUM CHLORIDE  0.13%


Medication Information

Warnings

For external use only

Avoid contact with eyes. In case of eye contact, flush eyes with water.

Uses
  • For handwashing to reduce bacteria on the skin. Recommended for repeated use.
Purpose

Antibacterial

Directions
  • Apply foam sanitizer to hands.
  • Rub over surfaces of both hands for 15 seconds.
  • No rinsing required.
Inactive Ingredients

Water, Coco-Glucoside, Laurtrimonium Chloride, Cocamidopropylamine Oxide, Citric Acid, Fragrance.

Description

BENZALKONIUM CHLORIDE  0.13%

Section 50565-1

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Section 50566-9

Stop use and ask a doctor if irritation or redness develops and persists.

Section 51945-4

Active Ingredient

BENZALKONIUM CHLORIDE  0.13%


Structured Label Content

Warnings

For external use only

Avoid contact with eyes. In case of eye contact, flush eyes with water.

Uses
  • For handwashing to reduce bacteria on the skin. Recommended for repeated use.
Purpose

Antibacterial

Directions
  • Apply foam sanitizer to hands.
  • Rub over surfaces of both hands for 15 seconds.
  • No rinsing required.
Inactive Ingredients (Inactive ingredients)

Water, Coco-Glucoside, Laurtrimonium Chloride, Cocamidopropylamine Oxide, Citric Acid, Fragrance.

Section 50565-1 (50565-1)

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Section 50566-9 (50566-9)

Stop use and ask a doctor if irritation or redness develops and persists.

Section 51945-4 (51945-4)

Active Ingredient (Active ingredient)

BENZALKONIUM CHLORIDE  0.13%


Advanced Ingredient Data


Raw Label Data

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