NDC 54748-702 Everyone Hand Sanitizer Wipes Lavender Aloe

Ethyl Alcohol

NDC Product Code 54748-702

NDC 54748-702-15

Package Description: 6 PACKET in 1 BOX > 15 PACKAGE in 1 PACKET (54748-702-16) > 4.17 mL in 1 PACKAGE

NDC Product Information

Everyone Hand Sanitizer Wipes Lavender Aloe with NDC 54748-702 is a a human over the counter drug product labeled by Eo Products, Llc. The generic name of Everyone Hand Sanitizer Wipes Lavender Aloe is ethyl alcohol. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Eo Products, Llc

Dosage Form: Cloth - A large piece of relatively flat, absorbent material that contains a drug. It is typically used for applying medication or for cleansing.

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.

Everyone Hand Sanitizer Wipes Lavender Aloe 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.

  • ALCOHOL 62 mL/100mL

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.

  • WATER (UNII: 059QF0KO0R)
  • LAVENDER OIL (UNII: ZBP1YXW0H8)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • CHAMOMILE (UNII: FGL3685T2X)
  • CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
  • WHITE TEA (UNII: O0M3396E09)
  • GLYCERIN (UNII: PDC6A3C0OX)

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.

Product Labeler Information

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

Labeler Name: Eo Products, Llc
Labeler Code: 54748
FDA Application Number: part333A 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: 01-25-2021 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: 12-31-2022 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.

Everyone Hand Sanitizer Wipes Lavender Aloe Product Label Images

Everyone Hand Sanitizer Wipes Lavender Aloe 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 Ingredients:

Ethanol 62%

Purpose:

Antiseptic

Uses:

  • For hand washing to decrease bacteria on skin.Recommended for repeated use.

Warnings:

  • Flammable, keep away from fire or flameFor external use onlyDo not use in eyes. If contact occurs, flush thoroughly with water.Stop use and ask doctor if irritation and redness develop and persists for more than 72 hours.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children. If swallowed, get medical help or contact the Poison Control center right away.

Directions:

  • Unfold towelette and wipe hands thoroughly for approximately 30 seconds.Do not use other than directed.

Other Information:

  • Store below 104°F (40°C)May discolor certain fabrics.

Inactive Ingredients:

Water, Lavandula Angustifolia (Lavender) Oil, **Aloe Barbadensis Leaf Juice, **Matricaria Recutita (Chamomile) Flower Extract, **Calendula Officinalis Flower Extract, **Camellia Sinensis (White Tea) Leaf Extract, Glycerin**organic

* Please review the disclaimer below.