NDC 72663-203 Welly Childrens Travel Medicine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
PINK (C48328)
12 MM
44596
44585
1
Code Structure Chart
Product Details
What is NDC 72663-203?
What are the uses for Welly Childrens Travel Medicine?
Which are Welly Childrens Travel Medicine UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40)
- DIPHENHYDRAMINE (UNII: 8GTS82S83M) (Active Moiety)
Which are Welly Childrens Travel Medicine 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CROSPOVIDONE (UNII: 2S7830E561)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- ETHYLCELLULOSE, UNSPECIFIED (UNII: 7Z8S9VYZ4B)
- FD&C BLUE NO. 1 ALUMINUM LAKE (UNII: J9EQA3S2JM)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MANNITOL (UNII: 3OWL53L36A)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- ACACIA (UNII: 5C5403N26O)
- STARCH, CORN (UNII: O8232NY3SJ)
- D&C RED NO. 27 ALUMINUM LAKE (UNII: ZK64F7XSTX)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
- HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
What is the NDC to RxNorm Crosswalk for Welly Childrens Travel Medicine?
- RxCUI: 1049900 - diphenhydrAMINE HCl 12.5 MG Chewable Tablet
- RxCUI: 1049900 - diphenhydramine hydrochloride 12.5 MG Chewable Tablet
- RxCUI: 313820 - acetaminophen 160 MG Chewable Tablet
- RxCUI: 313820 - APAP 160 MG Chewable Tablet
- RxCUI: 317865 - calcium carbonate 400 MG (Ca 170 MG) Chewable Tablet
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[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".