Escudo Ultra-Protect Original

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Escudo Ultra-Protect Original
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Indelpa, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 1cd4c38f-8156-bd74-e063-6394a90a9f56
SPL ID: 49f146b4-8bdf-2df2-e063-6294a90a95f6
Version: 3
Effective date: 2026-02-03
Source export date: 2026-10-27
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/29a1aba6a935d72bab5474118c2ccf25cb52dfe8488fe1593c734ea6c04e3722/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:45:04

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Escudo Ultra-Protect Original	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Indelpa, Inc	openfda.manufacturer_name
ndc	package	84529-001-01	openfda.package_ndc
ndc	product	84529-001	openfda.product_ndc
ndc11	package	84529000101	derived:openfda.package_ndc
rxcui		1926450	openfda.rxcui
spl id		49f146b4-8bdf-2df2-e063-6294a90a95f6	id
spl set id		1cd4c38f-8156-bd74-e063-6394a90a9f56	set_id
unii		F5UM2KM3W7	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

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.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.