ESCUDO ULTRA-PROTECT ORIGINAL- benzalkonium chloride soap

Escudo Ultra-Protect Original by

Drug Labeling and Warnings

Escudo Ultra-Protect Original by is a Otc medication manufactured, distributed, or labeled by Indelpa, Inc. 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 becateria on the skin.

Warnings

For external use only.

Do not use if

you are allergic to any of the ingredients

Directions

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

When using this product

avoid contact with eyes. In case of eye contact, rinse thoroughly with water.

Stop use and ask a doctor if

irritation or redness develop and persist for more than 72 hours.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Inactive Ingredients

Alcohol, D&C Red 33, Etidronic Acid, FD&C Green 3, Glycerin, Sodium Chloride, Sodium Palmate, Sodium Palm Kernelate, Tetrasodium EDTA, Titanium Dioxide, Water, Fragance.

Questions or Comments?

1-800-678-5082 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

Fresh clean scent
Deep cleansing

Escudo®

ULTRA-PROTECT

ORIGINAL

ANTIBACTERIAL BAR SOAP

NET WT 4.05 Z (115g)

INGREDIENTS AND APPEARANCE

ESCUDO ULTRA-PROTECT ORIGINAL 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84529-001
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
WATER (UNII: 059QF0KO0R)
ETIDRONIC ACID (UNII: M2F465ROXU)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
EDETATE SODIUM (UNII: MP1J8420LU)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FRAGRANCE 13576 (UNII: 5EM498GW35)
SODIUM PALMATE (UNII: S0A6004K3Z)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
ALCOHOL (UNII: 3K9958V90M)
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)

Product Characteristics
Color	blue	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: 84529-001-01	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	07/09/2024

Labeler - Indelpa, Inc (033350230)