NDC 44019-911 Sting Relief Pad

NDC Product Code 44019-911

NDC 44019-911-01

Package Description: .42 mL in 1 POUCH

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Sting Relief Pad with NDC 44019-911 is a product labeled by Yinjing Medical Technology (shanghai) Co., Ltd.. The generic name of Sting Relief Pad is . The product's dosage form is and is administered via form.

Labeler Name: Yinjing Medical Technology (shanghai) Co., Ltd.

Dosage Form: -

Product Type: 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)

Product Labeler Information

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

Labeler Name: Yinjing Medical Technology (shanghai) Co., Ltd.
Labeler Code: 44019
Start Marketing Date: 08-23-2016 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: 12-31-2020 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: I 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.

Sting Relief Pad Product Label Images

Sting Relief Pad 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

Benzocaine 6.0% w/vIsopropyl Alcohol 70.0% v/v

Purpose

Topical AnalgesicAntiseptic

Uses

Prevent infection in minor scrapes and temporary relief of itching of insect bites

Warnings

-For external use only-Caution Flammable-Do Not Use in the eyes. If contact occurs, rinse throughly with water. -Stop Use if irritation, redness or other symptoms develop. Consult a doctor if condition persist or gets worse.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a poison control center right away.

Directions

Apply to affected area 3 or 4 times daily. For Adults and children 2 years of age and older. Children under 2 years: consult physician.

Inactive Ingridients

Purified Water

* Please review the disclaimer below.