RemeVerse Instant Foam Hand Sanitizer

Manufacturer: RemeVerse | Lexia LLC | Lexia, LLC
Effective date: 2024-12-16
Label type: HUMAN OTC DRUG LABEL
Version: 6
Source: full-release
Hydrated at: 2026-06-01 00:43:59

Label at a glance#

ProductRemeVerse Instant Foam Hand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure9 sections

Label contents#

Full prescribing information#

RemeVerse instant foam hand sanitizer

INACTIVE INGREDIENT SECTION

Water, cetrimonium chloride, cocamidopropyl PG-dimonium chloride phosphate, dihydroxyethyl cocamine oxide,
acetamidoethoxyethanol, citric acid, fragrance

RemeVerse Instant Foam Hand Sanitizer

DOSAGE & ADMINISTRATION SECTION

Pump small amount into palm of hand ▪ Rub thoroughly over
all surfaces of both hands ▪ Rub hands together briskly until
dry ▪ For children under 6, use only under adult supervision

Topical Antimicrobial

INDICATIONS & USAGE SECTION

Effective at eliminating many common harmful germs in as
little as 15 seconds ▪ Recommended for repeated use

Benzalkonium Chloride .1% Active

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride - .1%

Warnings:

WARNINGS SECTION

For external use only
When using this product avoid contact with eyes. In case
of eye contact, flush eyes with water.

Safety Warning

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness
develops, or if condition persists for more than 72 hours.

Warning - Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Purpose - Antimicrobial

OTC - PURPOSE SECTION

Antimicrobial

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RemeverseRemeverse Hand Sanitizer Label 300ml lower resolution.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70317-145-30	2025-08-01	C162847	48780-1	3b156c62-3322-fb37-e063-e6dba90a4e07	RemeVerse Instant Foam Hand Sanitizer
70317-145-30	2025-07-29	C162847	48780-1	3b156c62-3322-fb37-e063-e6dba90a4e07	RemeVerse Instant Foam Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70317-145-30	RemeVerse Instant Foam Hand Sanitizer	300 mL in 1 BOTTLE, DISPENSING	LIQUID	300		6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70317-145	REMEVERSE INSTANT FOAM HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [REMEVERSE]	6	Legacy NDC, 1 package rows	20241218_a11299ca-3e05-f3cb-e053-2995a90a92e2.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

RemeVerse Instant Foam Hand Sanitizer
Benzalkonium Chloride
DIHYDROXYETHYL COCAMINE OXIDE
ANHYDROUS CITRIC ACID
FRAGRANCE LAVENDER & CHIA F-153480
BENZALKONIUM
CETRIMONIUM CHLORIDE
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70317-145	70317-145-30

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
DIHYDROXYETHYL COCAMINE OXIDE	8AR51R3BL5	IACT
ANHYDROUS CITRIC ACID	XF417D3PSL	IACT
FRAGRANCE LAVENDER & CHIA F-153480	SXS9CO2TZK	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
CETRIMONIUM CHLORIDE	UC9PE95IBP	IACT
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE	H2KVQ74JM4	IACT

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
2969f42a-c10d-b2b4-e063-6294a90abbad			a11299ca-3e05-f3cb-e053-2995a90a92e2	2024-12-16	Warnings	Exact identifier spl id: 2969f42a-c10d-b2b4-e063-6294a90abbad spl set id: a11299ca-3e05-f3cb-e053-2995a90a92e2

Reported adverse events (FAERS/openFDA)#

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