NDC 81902-202 Zylotrol Plus

Lidocaine 4%, Menthol 1%, Isopropyl Alcohol

NDC Product Code 81902-202

NDC 81902-202-15

Package Description: 1 KIT in 1 CARTON * 1 g in 1 PATCH * 1 mL in 1 PACKET

NDC Product Information

Zylotrol Plus with NDC 81902-202 is a a human over the counter drug product labeled by Whitestone Products Llc. The generic name of Zylotrol Plus is lidocaine 4%, menthol 1%, isopropyl alcohol. The product's dosage form is kit and is administered via topical form.

Dosage Form: Kit - A packaged collection of related material.

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.

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)
  • 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: Whitestone Products Llc
Labeler Code: 81902
FDA Application Number: part348 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: 10-15-2021 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 - 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".

* Please review the disclaimer below.

Zylotrol Plus Product Label Images

Zylotrol Plus 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:

Lidocaine 4.00%Menthol 1.00%


For temporary relief of pain


  • For external use only.Avoid contact with eyes.If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician.

Do Not Use

  • In large quantities, particularly over raw surfaces or blistered areas.

If Pregnant Or Breast-Feeding,

Ask a health professional before use.

Keep Out Of Reach Of Children.

  • If swallowed, get medical help or contact a Poison Control Center right away.

Directions (Adults And Children Over 12 Years):

Clean and dry affected area.Remove patch from backing and apply to affected area.Use only one patch at a time, and maximum of four patches / day.Leave patch on affected area for up to 8 hoursDo not use patches for longer than five consecutive days,Children under 12 should consult physician prior to use.

Inactive Ingredients:

Water, Glycerol, Sodium Polyacrylate, Propylene Glycol, Polysorbate 80, Tartaric Acid, Dihydroxyaluminium Aminoacetate, Methylparaben

Active Ingredient

Isopropyl Alcohol 70% v/v


First Aid Antiseptic


For preparation of the skin prior to an injection


  • For external use only Flammable, keep away from fire or flame

Otc - Do Not Use

  • Do not use with electrocautery procedures Do not use in the eyes Do not apply to irritated skin

Otc - Stop Use

  • Stop use if pain, irritation, redness, or swelling occurs, discontinue use and consult a physician.

Otc - Keep Out Of Reach Of Children

  • Keep out from reach of children. If swallowed, get medical help or contact a Poison Control Center right away.


  • Open packet Remove pad Apply topically as needed to cleanse intended area. Discard after single use.

Other Information

  • Store at room temperature 59-86°F (15-30°C) Contents sterile in unopened, undamaged package

Inactive Ingredients

Purified water

* Please review the disclaimer below.