NDC 41250-805 First Aid Antiseptic

Product Information

Product Code41250-805
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
First Aid Antiseptic
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Meijer
Labeler Code41250
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
03-07-2013
Listing Expiration Date 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.
12-31-2019
Exclude Flag 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".
I
NDC Code Structure

Usage Information


Product Packages

NDC 41250-805-04

Package Description: 148 mL in 1 BOTTLE

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

Product Details

First Aid Antiseptic is product labeled by Meijer. The product's dosage form is and is administered via form.


What are First Aid Antiseptic Active Ingredients?

The following is the list of active ingredients in this product. An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

  • LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
  • LIDOCAINE (UNII: 98PI200987) (Active Moiety)
  • BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
  • BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)


NDC to RxNorm Crosswalk

What is RxNorm? RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct code indicates a single concept unique identifier (RXCUI) is associated with this product:


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.

  • DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
  • EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • NONOXYNOL-9 (UNII: 48Q180SH9T)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
  • WATER (UNII: 059QF0KO0R)


* Please review the disclaimer below.

First Aid Antiseptic Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Active Ingredients                   Purpose



Benzalkonium 0.13%                First Aid Antiseptic

Lidocaine HCl 2.5%                 Pain Relieving Spray


Uses



First aid to help prevent bacterial contamination or skin infection, and for temporary relief of pain and itching associated with minor: cuts, scrapes, burns, sunburn, skin irritations


Warnings



​For external use only


​Ask A Doctor Before Use If You Have



  • deep or puncture wounds
  • animal bites
  • serious burns

When Using This Product​



  • do not use in or near the eyes
  • do not apply over large area of the body or in large quantities
  • do not apply over raw surfaces or blistered areas

​Stop Use And Ask A Doctor If



  • condition worsens
  • symptoms persist for more than 7 days, or clear up and occur again within a few days

​Keep Out Of Reach Of Children



​If swallowed get medical help or contact a Poison Control Center right away


Directions



• Adults and children 2 years and older: clean the affected area. Apply small amount on the area 1-3 times daily; may be covered with a sterile bandage (let dry first) • Children Under 2 years: Consult a physician.


Other Information



Avoid excessive heat


Inactive Ingredients



Diazolidinyl Urea, Disodium EDTA, Fragrance, Methylparaben, Nonoxynol 9, Propylene Glycol, Propylparaben, Sodium Phosphate Dibasic, Water


* Please review the disclaimer below.