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

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.

  • NONOXYNOL-9 (UNII: 48Q180SH9T)
  • 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 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.

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


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


​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


• 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.