I.C. Sanitizer and Re-Moisturizer with Benzalkonium Chloride

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: I.C. Sanitizer and Re-Moisturizer with Benzalkonium Chloride
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: R & R Lotion, Inc
Product type: HUMAN OTC DRUG
SPL set ID: cc5f24c8-fb85-49bd-8f55-4ec72fc0ffff
SPL ID: c4b804b7-76b9-4d09-aeb1-f0b99ea9f0e1
Version: 6
Effective date: 2025-09-10
Source export date: 2026-10-12
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:47:28

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 · 27 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		I.C. Sanitizer and Re-Moisturizer with Benzalkonium Chloride	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		R & R Lotion, Inc	openfda.manufacturer_name
ndc	package	59555-903-16	openfda.package_ndc
ndc	package	59555-903-09	openfda.package_ndc
ndc	package	59555-903-10	openfda.package_ndc
ndc	package	59555-903-13	openfda.package_ndc
ndc	package	59555-903-07	openfda.package_ndc
ndc	package	59555-903-11	openfda.package_ndc
ndc	package	59555-903-08	openfda.package_ndc
ndc	package	59555-903-04	openfda.package_ndc
ndc	package	59555-903-14	openfda.package_ndc
ndc	product	59555-903	openfda.product_ndc
ndc11	package	59555090311	derived:openfda.package_ndc
ndc11	package	59555090313	derived:openfda.package_ndc
ndc11	package	59555090314	derived:openfda.package_ndc
ndc11	package	59555090308	derived:openfda.package_ndc
ndc11	package	59555090309	derived:openfda.package_ndc
ndc11	package	59555090310	derived:openfda.package_ndc
ndc11	package	59555090316	derived:openfda.package_ndc
ndc11	package	59555090304	derived:openfda.package_ndc
ndc11	package	59555090307	derived:openfda.package_ndc
rxcui		1046442	openfda.rxcui
spl id		c4b804b7-76b9-4d09-aeb1-f0b99ea9f0e1	id
spl set id		cc5f24c8-fb85-49bd-8f55-4ec72fc0ffff	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 When using this product, avoid contact with eyes In case of eye contact, flush with water Keep out of reach of children, except under adult supervision If swallowed, get medical help Discontinue use if skin irritation or redness develops Do not use on broken skin

Reported adverse events (FAERS/openFDA)#

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