NDC 41250-805 First Aid Antiseptic

NDC Product Code 41250-805

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.

NDC Product Information

First Aid Antiseptic with NDC 41250-805 is a product labeled by Meijer. The generic name of First Aid Antiseptic is . The product's dosage form is and is administered via form.

Labeler Name: Meijer

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.

  • 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)

Product Labeler Information

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

Labeler Name: Meijer
Labeler Code: 41250
Start Marketing Date: 03-07-2013 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: 12-31-2019 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 - INACTIVATED, the listing data was inactivated by the FDA. 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.

First Aid Antiseptic Product Label Images

First Aid Antiseptic 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                   Purpose

Benzalkonium 0.13%                First Aid AntisepticLidocaine 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 woundsanimal bitesserious burns

When Using This Product​

  • Do not use in or near the eyesdo not apply over large area of the body or in large quantitiesdo not apply over raw surfaces or blistered areas

​Stop Use And Ask A Doctor If

  • Condition worsenssymptoms 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.