NDC 69842-404 Cvs Health Medication And Topical Refill Pouch
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69842 - Cvs
- 69842-404 - Cvs Health Medication And Topical Refill Pouch
Product Characteristics
WHITE (C48325)
ROUND (C48348)
11 MM
AZ;234
44;157;ASPIRIN
Product Packages
NDC Code 69842-404-00
Package Description: 1 KIT in 1 BAG * 2 TABLET in 1 PACKAGE (52124-0014-1) * .5 g in 1 TUBE (52124-0003-1) * .8 mL in 1 PACKAGE (52124-0001-1) * 2 TABLET in 1 PACKET (52124-0015-1) * .7 mL in 1 PACKAGE (44224-0001-2) * .7 mL in 1 PACKAGE (52124-0017-1) * 2 CAPSULE in 1 PACKET (52124-0016-1)
Product Details
What is NDC 69842-404?
What are the uses for Cvs Health Medication And Topical Refill Pouch?
Which are Cvs Health Medication And Topical Refill Pouch UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40)
- DIPHENHYDRAMINE (UNII: 8GTS82S83M) (Active Moiety)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
- AMMONIA (UNII: 5138Q19F1X)
- AMMONIA (UNII: 5138Q19F1X) (Active Moiety)
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (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)
Which are Cvs Health Medication And Topical Refill Pouch 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:
- GELATIN (UNII: 2G86QN327L)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- STARCH, CORN (UNII: O8232NY3SJ)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- WATER (UNII: 059QF0KO0R)
- DIMETHICONE 1000 (UNII: MCU2324216)
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- C12-13 ALCOHOLS (UNII: T7ZJT3I9X2)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PETROLATUM (UNII: 4T6H12BN9U)
- MINERAL OIL (UNII: T5L8T28FGP)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
What is the NDC to RxNorm Crosswalk for Cvs Health Medication And Topical Refill Pouch?
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 1.3 MG/ML Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Topical Swab
- RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Pad
- RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Swab
* 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".