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

Key Label Information#

Active Ingredients And Purpose

Purpose

Antimicrobial

Active Ingredient

Benzalkonium Chloride 0.13%

Uses

Uses

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

Warnings

Warnings

For external use only.

Directions And Dosage

Directions

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

Other Label Information

Inactive Ingredients

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.

PDP

MEDILAB 365 HAND SANITIZER FOAM ANTI-BACTERIAL ADVANCED FORMULA KILLS 99.99% OF GERMS REGISTERED CERTIFIED FDA GMP FORMULA FACILITY 5 FL.OZ (150 ML)

Label Images#

Hand Sanitizer Foam 16 fl.oz.-1
Hand Sanitizer Foam 16 fl.oz.-1
Hand Sanitizer Foam 5 fl.oz.-1
Hand Sanitizer Foam 5 fl.oz.-1
Hand Sanitizer Foam 1.7 fl.oz.-1
Hand Sanitizer Foam 1.7 fl.oz.-1

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#

NDC Codes#

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

Ingredients#

Complete SPL Sections#

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 O F.

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

MEDILAB 365 HAND SANITIZER FOAM ANTI-BACTERIAL ADVANCED FORMULA KILLS 99.99% OF GERMS REGISTERED CERTIFIED FDA GMP FORMULA FACILITY 5 FL.OZ (150 ML)

Source Document#

Source XML