NDC 72471-101 Antimicrobial

Antimicrobial Face And Body Spray

NDC Product Code 72471-101

NDC 72471-101-10

Package Description: 1 g in 1 BOTTLE, PLASTIC

NDC Product Information

Antimicrobial with NDC 72471-101 is a a human over the counter drug product labeled by Vmp Cosmetics. The generic name of Antimicrobial is antimicrobial face and body spray. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Vmp Cosmetics

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Antimicrobial Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • BENZALKONIUM CHLORIDE .13 g/100g

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • 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)
  • ECHINACEA PURPUREA (UNII: QI7G114Y98)
  • OREGANO (UNII: 0E5AT8T16U)
  • HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • WATER (UNII: 059QF0KO0R)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • HYALURONIC ACID (UNII: S270N0TRQY)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • GLYCYRRHIZA URALENSIS (UNII: 42B5YD8F0K)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Vmp Cosmetics
Labeler Code: 72471
FDA Application Number: part333E What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 09-21-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Antimicrobial Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

ACTIVE INGREDIENTBenzalkonium Chloride 0.13%

Purpose Section

PURPOSEAntiseptic

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

MEDILAB365FACE & BODY SPRAYANTI-BACTERIALADVANCED HYDRATING FORMULAKILLS 99.99%OF GERMS3.3 FL. OZ. (100ML)

* Please review the disclaimer below.