NDC 71504-659 Bearicaid Antiseptic Skin Sanitizing Wipes

Ethyl Alcohol

NDC Product Code 71504-659

NDC 71504-659-01

Package Description: 3.48 mL in 1 PACKET

NDC 71504-659-58

Package Description: 150 PACKET in 1 BOX > 3.48 mL in 1 PACKET

NDC 71504-659-66

Package Description: 50 PACKET in 1 BOX > 3.48 mL in 1 PACKET

NDC Product Information

Bearicaid Antiseptic Skin Sanitizing Wipes with NDC 71504-659 is a a human over the counter drug product labeled by Knet Systems Corp.. The generic name of Bearicaid Antiseptic Skin Sanitizing Wipes is ethyl alcohol. The product's dosage form is cloth and is administered via topical form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1251416.

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.

Bearicaid Antiseptic Skin Sanitizing Wipes 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.


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.

  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • CHAMOMILE (UNII: FGL3685T2X)
  • CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
  • TEA TREE OIL (UNII: VIF565UC2G)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • WATER (UNII: 059QF0KO0R)

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: Knet Systems Corp.
Labeler Code: 71504
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: 06-14-2017 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

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Bearicaid Antiseptic Skin Sanitizing Wipes Product Label Images

Bearicaid Antiseptic Skin Sanitizing Wipes 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

Ethyl Alcohol 65.9% by volume

Purpose

Antimicrobial

​Uses

•  Helps Prevent the risk of cross contamination of bacteria that potentially can cause disease or infection•  To decrease bacteria on the skin•  Recommended for repeated use•  Dries in seconds

​Warnings

•  Flammable, keep away from fire or flame•  For external use only•  Do not use​ if irritation or redness develop. If condition persists for longer than 72 hours consult a physician.

​Directions

•  Tear open packet and remove cloth wipe•  Wipe hands, fingers and wrists areas thoroughly for 15 seconds•  For heavy soil, use first wipe to clean hands and sanitize with a second wipe•  Children under 6 should be supervised when using this product•  Dispose of used cloth properly

Inactive Ingredients

SkinscreenEX……………..Aloe Barbadensis Leaf Juice Powder, Chamomilla Recutita flower Extract, Chlorhexidine Digluconate, Fragrance, Melaleuca Alternifolia Leaf Oil, Triethanolamine, Water

Other

Contains SkinscreenEx special blend with essential oils to support healthy skinUse directly on the hands and skin to CLEAN, SANITIZE, and REDUCE bacteria that can potentially cause diseaseSanitizes and Cleans with HYGENIC GRADE EMBOSSED 6 X 6 CLOTHRECOMMENDED SAFE FOR DAILY USE50 INDIVIDUALLY SEALED PACKETSKeeping hands clean is one of the best things you can do to keep from getting sickEffectively Removes 99.99% of Germs AND Helps Reduce the Bacteria that can Potentially Cause DiseaseEFFECTIVE AGAINST:MRSASTAPHE.COLIALSO HELPS REDUCE E.COLI BACTERIA ASSOCIATED WITH THE FOLLOWING SYMPTOMS:• PNEUMONIA• EAR INFECTIONS• BACTERIAL DIARRHEA• URINARY TRACT• INFECTIONS• BACTERIAL (E.COLI) STOMACH FLU• VOMITING• FEVER• NAUSEABearicaid does not contain triclosan, parabens, sulfates, or phthalatesManufactured for: BEARICAID APPLIED SCIENCESLos Angeles, CA 91331, Designed in USAMade in China

* Please review the disclaimer below.