NDC 0924-5701 First Aid And Burn

NDC Product Code 0924-5701

NDC 0924-5701-02

Package Description: 6 PACKET in 1 BAG > .9 g in 1 PACKET (0924-5701-01)

NDC 0924-5701-03

Package Description: 6 PACKET in 1 BAG > .9 g in 1 PACKET (0924-5701-01)

NDC 0924-5701-04

Package Description: 10 PACKET in 1 BOX > .9 g in 1 PACKET (0924-5701-01)

NDC 0924-5701-05

Package Description: 12 PACKET in 1 BOX > .9 g in 1 PACKET (0924-5701-01)

NDC 0924-5701-06

Package Description: 25 PACKET in 1 BOX > .9 g in 1 PACKET (0924-5701-01)

NDC 0924-5701-07

Package Description: 60 PACKET in 1 BOX > .9 g in 1 PACKET (0924-5701-01)

NDC 0924-5701-08

Package Description: 144 PACKET in 1 BOX > .9 g in 1 PACKET (0924-5701-01)

NDC 0924-5701-09

Package Description: 10 PACKET in 1 BOX > .9 g in 1 PACKET (0924-5701-01)

NDC 0924-5701-10

Package Description: 12 PACKET in 1 BOX > .9 g in 1 PACKET (0924-5701-01)

NDC 0924-5701-11

Package Description: 25 PACKET in 1 BOX > .9 g in 1 PACKET (0924-5701-01)

NDC 0924-5701-12

Package Description: 144 PACKET in 1 BOX > .9 g in 1 PACKET (0924-5701-01)

NDC 0924-5701-13

Package Description: 60 PACKET in 1 BOX > .9 g in 1 PACKET (0924-5701-01)

This product is EXCLUDED from the official NDC directory because the listing certification is expired.

NDC Product Information

First Aid And Burn with NDC 0924-5701 is a product labeled by Acme United Corporation. The generic name of First Aid And Burn is . The product's dosage form is and is administered via form.

Labeler Name: Acme United Corporation

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.

  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • ALCOHOL (UNII: 3K9958V90M)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • MINERAL OIL (UNII: T5L8T28FGP)
  • PARAFFIN (UNII: I9O0E3H2ZE)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • WATER (UNII: 059QF0KO0R)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • WHITE WAX (UNII: 7G1J5DA97F)

Product Labeler Information

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

Labeler Name: Acme United Corporation
Labeler Code: 0924
Start Marketing Date: 01-27-2012 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: 12-31-2018 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: E 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 And Burn 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

Other

Drug Facts

Active Ingredients

Benzalkonium Chloride 0.13%
Lidocaine HCl 0.5%

Purpose

First Aid Antiseptic
External analgesic

Uses

  • First aid to help prevent infection and for the temporary relief of itching associated with
  • Minor cuts
  • Scrapes
  • Burns

Warnings

For external use only

Do Not Use

  • In the eyes or apply over large areas of the body
  • Longer than 1 week unless directed by a doctor
  • In large quantities, particularly over raw surfaces or blistered areas

Otc - Ask Doctor

Ask a doctor before use if you have deep or puncture wounds, animal bites, or serious burns

Otc - When Using

When using this product avoid contact with eyes

Stop Use And Ask A Doctor If

  • Condition worsens or persists for more than 7 days
  • Clears up and occurs again within a few days

Otc - Keep Out Of Reach Of Children

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 of age and older:
  • Clean the affected area
  • Apply a small amount of this product to the area 1 to 3 times daily
  • May be covered with a sterile bandage
  • Children under 2 years of age: consult a doctor

Other Information

  • Store at room temperature
  • Do not use if packet is opened or torn

Inactive Ingredients

Aloe vera, emulsifying wax, ethyl alcohol, methylparaben, mineral oil, paraffin, propylparaben, purified water, white petrolatum, white wax

Questions? 1-800-835-2263

REORDERwww.PhysiciansCareFirstAid.com1 800 835 2263

* Please review the disclaimer below.