NDC 69842-300 Cvs All Purpose First Aid Kit
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
RED (C48326 - REDDISH BROWN)
WHITE (C48325 - WHITE)
10 MM
G;2
TCL;011
Code Structure Chart
Product Details
What is NDC 69842-300?
What are the uses for Cvs All Purpose First Aid Kit?
Which are Cvs All Purpose First Aid Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMMONIA (UNII: 5138Q19F1X)
- AMMONIA (UNII: 5138Q19F1X) (Active Moiety)
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- IBUPROFEN (UNII: WK2XYI10QM)
- IBUPROFEN (UNII: WK2XYI10QM) (Active Moiety)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
- BACITRACIN ZINC (UNII: 89Y4M234ES)
- BACITRACIN (UNII: 58H6RWO52I) (Active Moiety)
- NEOMYCIN SULFATE (UNII: 057Y626693)
- NEOMYCIN (UNII: I16QD7X297) (Active Moiety)
- POLYMYXIN B SULFATE (UNII: 19371312D4)
- POLYMYXIN B (UNII: J2VZ07J96K) (Active Moiety)
- ASPIRIN (UNII: R16CO5Y76E)
- ASPIRIN (UNII: R16CO5Y76E) (Active Moiety)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
Which are Cvs All Purpose 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:
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- C12-13 ALCOHOLS (UNII: T7ZJT3I9X2)
- WATER (UNII: 059QF0KO0R)
- DIMETHICONE 1000 (UNII: MCU2324216)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- GLYCERIN (UNII: PDC6A3C0OX)
- MENTHOL (UNII: L7T10EIP3A)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- POVIDONE (UNII: FZ989GH94E)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- STARCH, CORN (UNII: O8232NY3SJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- POVIDONE K30 (UNII: U725QWY32X)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- TALC (UNII: 7SEV7J4R1U)
- PETROLATUM (UNII: 4T6H12BN9U)
- MINERAL OIL (UNII: T5L8T28FGP)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
What is the NDC to RxNorm Crosswalk for Cvs All Purpose First Aid Kit?
- RxCUI: 1009433 - lidocaine HCl 2.5 % Topical Gel
- RxCUI: 1009433 - lidocaine hydrochloride 0.025 MG/MG Topical Gel
- RxCUI: 1009433 - lidocaine hydrochloride 2.5 % Topical Gel
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 1.3 MG/ML Medicated Pad
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[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".