ANTIMICROBIAL- antimicrobial face and body spray liquid

Antimicrobial by

Drug Labeling and Warnings

Antimicrobial by is a Otc medication manufactured, distributed, or labeled by VMP Cosmetics. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENT

Benzalkonium Chloride 0.13%

PURPOSE SECTION

PURPOSE

Antiseptic

USES

To help reduce bacteria on the skin

WARNINGS

For external use only

When using this product

*avoid contact with eyes. If eye contact occurs, flush thoroughly with water.

Stop use

Stop use and consult with a doctor. If irritation or redness develops.

Keep Out of Reach of Children

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

Directions * Apply a few sprays directly into the face and bodyas often as needed. Allow to dry without wiping. Safe to spray on clothes. Safe to use all day long.

Other Information

Do not store above 104º F.

Inactive Ingredients

Agua (Water),Glycerin, Butylene Glycol, Hyaluronic Acid, Aloe Barbadensis Leaf Juice, Echinacea Purpurea, Sambucus Nigra Fruit, GlycyrrhizaUralensis (Licorice), Origanum Vulgare (Oregano) Leaf, HypericumPerforatum, Uncaria Tomentosa, Polysorbate 20, Citric Acid, Tetrasodium EDTA, Ethylhexylglycerin, Phenoxyethanol, Fragrance.

PDP

MEDILAB

365

FACE & BODY SPRAY

ANTI-BACTERIAL

ADVANCED HYDRATING FORMULA

KILLS 99.99%

OF GERMS

3.3 FL. OZ. (100ML)

INGREDIENTS AND APPEARANCE

ANTIMICROBIAL 
antimicrobial face and body spray liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72471-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EUROPEAN ELDERBERRY (UNII: BQY1UBX046)
UNCARIA TOMENTOSA LEAF (UNII: 487U8M3D2P)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE SODIUM (UNII: MP1J8420LU)
WATER (UNII: 059QF0KO0R)
ECHINACEA PURPUREA (UNII: QI7G114Y98)
OREGANO (UNII: 0E5AT8T16U)
HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCYRRHIZA URALENSIS (UNII: 42B5YD8F0K)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
HYALURONIC ACID (UNII: S270N0TRQY)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72471-101-10	1 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	09/21/2020

Labeler - VMP Cosmetics (022451337)

Registrant - VMP Cosmetics (022451337)

Establishment
Name	Address	ID/FEI	Business Operations
VMP Cosmetics		022451337	manufacture(72471-101)