ESCUDO ULTRA-PROTECT SOFT CARE- benzalkonium chloride soap

Escudo Ultra-Protect Soft Care by

Drug Labeling and Warnings

Escudo Ultra-Protect Soft Care by is a Otc medication manufactured, distributed, or labeled by Indelpa, Inc., HADA International SAS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Active ingredient------------------------- Purpose

Benzalkonium Chloride 0.1% .......... Antibacterial

Active ingredient -------------------------Purpose

Benzalkonium Chloride 0.1% .......... Antibacterial

Use

For washing to decrease bacteria on the skin.

Uses

for washing to decrease bacteria on the skin.

Warnings

For external use only.

Do not use

Do not use if you are allergic to any of the ingredients.

When using this product

When using this product avoid contact with eyes. In case of eye contact, rinse thoroughly with water.

Stop use and ask a doctor

Stop use and ask a doctor if irritation or redness develop and persist for more than 72 hours.

Keep out of reach of children

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

Directions

• Wet bar with water.
• Lather vigorously and wash skin.
• Rinse with water and dry throughly.

Inactive ingredients

Alcohol, Benzyl Benzoate, Etidronic Acid, Glycerin, Sodium Chloride, Sodium Kernelate, Sodium Palmate, Tetrasodium EDTA, Titanium Dioxide, Water, Fragrance.

Questions or Comments?

1-800-678-5082 I info@indelpa.com.mx

SPL UNCLASSIFIED SECTION

*effective only against E. coli and S. Aureus.

Distributed by Indelpa, Inc.

18911 Hardy Oak Blvd Suite 327

San Antonio, TX 78258.

MADE IN COLOMBIA

Package Label principal display panel

Eliminates 99.9%

of Bacteria

• Gentle on skin
• Deep cleansing

SOFT CARE

Escudo®

ULTRA-PROTECT

ANTIBACTERIAL BAR SOAP

NET WT 4.05 Z (115g)

INGREDIENTS AND APPEARANCE

ESCUDO ULTRA-PROTECT SOFT CARE 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84529-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
FRAGRANCE 13576 (UNII: 5EM498GW35)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ETIDRONIC ACID (UNII: M2F465ROXU)
SODIUM PALMATE (UNII: S0A6004K3Z)
GLYCERIN (UNII: PDC6A3C0OX)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
BENZYL BENZOATE (UNII: N863NB338G)
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
EDETATE SODIUM (UNII: MP1J8420LU)

Product Characteristics
Color	white	Score	no score
Shape	FREEFORM	Size	96mm
Flavor		Imprint Code	Escudo;ULTRA;PROTECT
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84529-002-01	115 g in 1 CELLO PACK; Type 0: Not a Combination Product	07/09/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	07/08/2024

Labeler - Indelpa, Inc. (033350230)

Establishment
Name	Address	ID/FEI	Business Operations
HADA International SAS		882405152	manufacture(84529-002)