NDC 0498-4238 4238 First Aid Kit

4238 First Aid Kit

NDC Product Code 0498-4238

NDC 0498-4238-01

Package Description: 1 KIT in 1 KIT * .4 mL in 1 POUCH (0498-0143-04) * .3 mL in 1 POUCH (0498-0121-00) * .4 mL in 1 POUCH (0498-0733-00) * 30 mL in 1 BOTTLE (0498-0100-01) * .9 g in 1 PACKET

NDC Product Information

4238 First Aid Kit with NDC 0498-4238 is a a human over the counter drug product labeled by Honeywell Safety Products Usa, Inc. The generic name of 4238 First Aid Kit is 4238 first aid kit. The product's dosage form is kit and is administered via form.

Labeler Name: Honeywell Safety Products Usa, Inc

Dosage Form: Kit - A packaged collection of related material.

Product Type: Human Otc Drug 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.

  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • WATER (UNII: 059QF0KO0R)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • PEG-100 STEARATE (UNII: YD01N1999R)
  • LIGHT MINERAL OIL (UNII: N6K5787QVP)
  • EDETIC ACID (UNII: 9G34HU7RV0)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
  • SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
  • WATER (UNII: 059QF0KO0R)
  • NONOXYNOL-9 (UNII: 48Q180SH9T)
  • WATER (UNII: 059QF0KO0R)
  • MENTHOL (UNII: L7T10EIP3A)
  • WATER (UNII: 059QF0KO0R)
  • BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)

Product Labeler Information

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

Labeler Name: Honeywell Safety Products Usa, Inc
Labeler Code: 0498
Marketing Category: UNAPPROVED DRUG OTHER - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 03-14-2019 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: N 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.

4238 First Aid Kit 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

First Aid Burn Cream Active Ingredient

Benzalkonium chloride o.13%Lidocaine HCl 0.5%

First Aid Burn Cream Purpose

First aid antisepticExternal analgesic

First Aid Burn Cream Uses

  • Prevent skin infectionfor temporary relief of pain associated with minor burns

First Aid Burn Cream Warnings

For external use only

Do Not Use

  • In or near the eyesif you are allergic to any of the ingredientsin large areas of the body, particularly over raw surfaces or blistered areasfor more than 10 days

  • In the eyes over large areas of the body

  • If solution changes color or becomes cloudyif you have open wounds in or near the eyes, get medical help right away.

  • In the eyesover large areas of the bodyon individuals who are allergic or sensitive to iodine

  • Over large areas of the bodyin eyesover raw or blistered areas

Ask A Doctor Before Use If You Have

  • Deep or puncture woundsanimal bitesserious burns

  • Deep or puncture woundsanimal bitesserious burn

  • Deep or puncture wounds,animal bitesserious burns

Stop Use And Ask A Doctor If

  • Condition worsenssymptoms persist for more than 7 days or clear up and occurs again within a few days

  • You experience eye painchanges in visioncontinued redness or irritation of the eyecondition worsens or persists

  • Conditions persists or gets worseirritation and redness develops

First Aid Burn Cream Directions

  • Adults and children 2 years of age and older:clean the affected areaapply a small amount of this product (equal to the surface area of the tip of a finger) onto affected area 1 to 3 times dailymay be covered with a sterile bandagechildren under 2 years of age: consult a doctor

First Aid Burn Cream Other Information

  • Tamper evident sealed packetsdo not use if packet is opened or torn

First Aid Burn Cream Inactive Ingredients

Aloe barbadensis juice, cetyl alcohol, diazolidinyl urea, edetate disodium, glycerin, glyceryl stearate SE, methylparaben, mineral oil, PEG-100, propylene glycol, propylparaben, stearic acid, trolamine, water

First Aid Burn Cream Questions

1-800-430-5490

Alcohol Wipe Active Ingredient

Isopropyl alcohol 70%

Alcohol Wipe Purpose

First aid antiseptic

Alcohol Wipe Uses

  • First aid to help prevent infection in minor cuts, scrapes, and burns

Alcohol Wipe Warnings

For external use only

When Using This Product

  • Do not use longer than one week unless directed by a doctor

  • Do not use longer than one wek unless directed by a doctor

Stop Use And Consult A Doctor

  • If condition persists or gets worse

Keep Out Of Reach Of Children

  • If swallowed, get medical help or contact a Poison Control Center right away.

  • If swallowed, get medical help or contact a Poison Control Center right away.

  • If swallowed, get medical help or contact a Poison Control Center right away.

Alcohol Wipe Directions

  • Clean the affected areaapply wipe to affected area 1 to 3 times dailymay be covered with a sterile bandagediscard wipe after single use

Alcohol Wipe Other Information

Store at room temperature 15
0 to 25
0 C (59
0 to 77
0F)

Alcohol Wipe Inactive Ingredient

Water

Alcohol Wipe Questions

1-800-430-5490

Eyewash Active Ingredient

Sterile Water 99%

Eyewash Purpose

Eyewash

Eyewashuses

  • For flushing the eye to remove loose foreign material, air pollutants or chlorinated water

Eyewash Warnings

For external use only Obtain immediate medical treatment for all open wounds in or near eyes. To avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard.

Eyewash Directions

  • Remove contacts before usingtwist top to removeflush the affected area as neededcontrol rate of flow by pressure on the bottleif necessary, continue flushing with emergency eyewash or shower

Eyewash Inactive Ingredients

Sodium chloride, sodium phosphate dibasic, sodium phosphate monobasic

Eyewash Questions

1-800-430-5490

Pvp Active Ingredient

Povidone-iodine solution USP, 10% (equivalent to 1% titratable iodine)

Pvp Purpose

First aid antiseptic

Pvp Uses

  • First aid to help prevent the risk of infection in minor cuts, scrapes, and burns

Pvp Warnings

For external use only

Keep Out Of Reach Of Children.

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

Pvp Directions

  • Reverse cardboard sleeve, then crush at dot between thumb and forefinger. Allow solution to saturate tip and apply solution to injury.clean affected areaapply to affected area 1 to 3 times dailymay be covered with a sterile bandagediscard swab after single use

Pvp Other Informatiion

  • Store at room temperature away from lightkeep from freezing or excessive heat do not use if package is torn or open

Pvp Inactive Ingredient

Citric acid, disodium phosphate,nonoxynol-9, sodium hydroxide, water

Pvp Questions

1-800-430-5490

Sting Relief Active Ingredient (In Each Wipe)

Ethyl alcohol 50.0% Lidocaine HCl 2.0%

Sting Relief Purpose

Antiseptic
Topical pain relief

Sting Relief Uses

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

Sting Relief Warnings

For external use only

Flammable, keep away from open fire or flame

Stop Use And Ask A Doctor

  • If conditions worsen or persist for more than 7 days or clear up and occur again within a few days

Stig Relief Directions

Adults and children 2 years and older: Apply to cleaned affected area not more than 3 times daily.
children under 2 years of age: consult a doctor.

Sting Relief Inactive Ingredients

Benzalkonium chloride, menthol, and purified water

4238 013087-1725A Kit Contents

1 KNUCKLE BAND 8 PER1 FIRST AID BURN CREAM 6 PER1 TRIANGULAR BDG, NON-STERILE1 GAUZE PADS, 3" X 3", 4 PER1 ADH TAPE, .5" X 2.5 YD, 2 PER1 GAUZE COMPRESS, 1728 SQ IN 11 INSTANT COLD PACK 4" X 6"1 BUFFERED EYE WASH 1 OZ BTL1 BANDAGE COMP, 4" OFFSET, 1 PER1 ADHESIVE BDG,PLSTIC,1"X3"16PER1 PVP IODINE WIPES 10 PER1 NITRILE GLOVES 2PR BBP1 MICROSHIELD W/VNL GLV/ALCLLBL STOCK 6-3/8"X4"LBL STOCK 4"X2-7/8"1 LBL STOCK 3"x1-7/8"1 KIT STL 16 UN (VERTICAL)1 LABL INSTR FA REV A1 LBL CONTENTS ANSI Z308.1-2009 REV B1 STING Relief WIPES 10

* Please review the disclaimer below.

Previous Code
0498-4237
Next Code
0498-4239