Hand Sanitizer Foam

Manufacturer
VMP Cosmetics, LLC
Effective date
2022-01-22
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:47:26

Label at a glance#

ProductHand Sanitizer Foam
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

*To help decrease bacterial on the skin. Recomended for repeated use as needed.

Dosage and administration

* Pump a sufficient amount of foam into palm of hand. * Rub thoroughly over all surfaces of both hands. * Rub hands repeatedly until dry.

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

*To help decrease bacterial on the skin. Recomended for repeated use as needed.

Warnings

WARNINGS SECTION

For external use only.

Stop Use

OTC - STOP USE SECTION

*Stop use and consult with doctor if irritation and redness develops, or if condition persists for more than 24 hours.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or contact a poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

* Pump a sufficient amount of foam into palm of hand.

* Rub thoroughly over all surfaces of both hands.

* Rub hands repeatedly until dry.

Other Information

OTHER SAFETY INFORMATION

Do not store above 104 OF.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Hyaluronic Acid, Aloe Barbadensis Leaf Juice Powder, Quillaja Saponaria (Soapbark) Bark Extract, PEG-8 Dimethicone, Polyquaternium-7, PPG-26 Buteth-26, PEG-40 Hydrogenated Castor Oil, Sodium Decylglucosides Hydroxypropylsulfonate, Ethylhexylglycerin, Phenoxyethanol, Fragrance.

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabelLabelLabelMEDILAB

365

HAND SANITIZER FOAM

ANTI-BACTERIAL

ADVANCED FORMULA

KILLS 99.99%

OF GERMS

REGISTERED CERTIFIED

FDA GMP

FORMULA FACILITY

5 FL.OZ (150 ML)

Hand Sanitizer Foam 1.7 fl.oz.Hand Sanitizer Foam 1.7 fl.oz.

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN3
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD3
1020365benzalkonium chloride 0.13 % Topical FoamSY3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72471-100-20Hand Sanitizer Foam1 g in 1 BOTTLE, PLASTICLIQUID13
72471-100-21Hand Sanitizer Foam1 g in 1 BOTTLE, PLASTICLIQUID13
72471-100-22Hand Sanitizer Foam1 g in 1 BOTTLE, PLASTICLIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72471-100HAND SANITIZER FOAM (ANTI-BACTERIAL ADVANCED FORMULA) LIQUID [VMP COSMETICS, LLC]3Legacy NDC, 3 package rows20220123_aabc441a-89ef-2bf8-e053-2a95a90aba2d.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72471-10072471-100-20, 72471-100-21, 72471-100-22

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d626aba9-5956-4a05-e053-2995a90a82d9aabc441a-89ef-2bf8-e053-2a95a90aba2d2022-01-22WarningsExact identifier
spl id: d626aba9-5956-4a05-e053-2995a90a82d9
spl set id: aabc441a-89ef-2bf8-e053-2a95a90aba2d

Reported adverse events (FAERS/openFDA)#

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