NDC 0498-4204 4204 First Aid Kit
Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0498 - Honeywell Safety Products Usa, Inc
- 0498-4204 - 4204 First Aid Kit
Product Characteristics
RED (C48326 - RED)
OVAL (C48345)
22 MM
B
1
Product Packages
NDC Code 0498-4204-01
Package Description: 1 KIT in 1 KIT * 59 mL in 1 BOTTLE, SPRAY (0498-0221-59) * 1 LOZENGE in 1 POUCH (0498-1120-00) * .9 g in 1 PACKET (0498-0730-01) * 59 mL in 1 BOTTLE, SPRAY (0498-0402-59) * 118 mL in 1 BOTTLE (0498-0100-02) * 2 TABLET in 1 PACKET * .3 mL in 1 POUCH (0498-0121-00) * .4 mL in 1 POUCH (0498-0143-04)
Product Details
What is NDC 0498-4204?
What are the uses for 4204 First Aid Kit?
Which are 4204 First Aid Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- WATER (UNII: 059QF0KO0R) (Active Moiety)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
- POVIDONE-IODINE (UNII: 85H0HZU99M)
- IODINE (UNII: 9679TC07X4) (Active Moiety)
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
- NEOMYCIN SULFATE (UNII: 057Y626693)
- NEOMYCIN (UNII: I16QD7X297) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are 4204 First Aid Kit Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)
- WATER (UNII: 059QF0KO0R)
- NONOXYNOL-9 (UNII: 48Q180SH9T)
- STARCH, CORN (UNII: O8232NY3SJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- POVIDONE (UNII: FZ989GH94E)
- SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)
- EDETIC ACID (UNII: 9G34HU7RV0)
- GLYCERIN (UNII: PDC6A3C0OX)
- TROLAMINE (UNII: 9O3K93S3TK)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- OCTOXYNOL-9 (UNII: 7JPC6Y25QS)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- TEA TREE OIL (UNII: VIF565UC2G)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- OCTOXYNOL 9 (UNII: 7JPC6Y25QS)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- PETROLATUM (UNII: 4T6H12BN9U)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- CORN SYRUP (UNII: 9G5L16BK6N)
- SUCROSE (UNII: C151H8M554)
What is the NDC to RxNorm Crosswalk for 4204 First Aid Kit?
- RxCUI: 1039012 - benzalkonium chloride 0.13 % Topical Spray
- RxCUI: 1039012 - benzalkonium chloride 1.3 MG/ML Topical Spray
- RxCUI: 1053173 - water 98.6 % Ophthalmic Irrigation Solution
- RxCUI: 1053173 - water 986 MG/ML Ophthalmic Irrigation Solution
- RxCUI: 1053173 - water 98.577 % Ophthalmic Irrigation Solution
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[3] 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.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] 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.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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] 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".