NDC 72663-205 Welly Travel Medicine Kit
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72663 - Welly Health Pbc
- 72663-205 - Welly Travel Medicine Kit
Product Characteristics
BROWN (C48332)
PINK (C48328)
GREEN (C48329 - LIGHT)
BLUE (C48333)
OVAL (C48345)
10 MM
14 MM
44291
44608
44375
44386
2
Product Packages
NDC Code 72663-205-48
Package Description: 1 KIT in 1 KIT * 2 BLISTER PACK in 1 KIT (72663-746-48) / 6 TABLET, CHEWABLE in 1 BLISTER PACK * 12 TABLET in 1 BLISTER PACK (72663-567-48) * 8 TABLET in 1 BLISTER PACK (72663-369-48) * 16 TABLET in 1 BOTTLE (72663-428-48) * 8 TABLET in 1 BLISTER PACK (72663-632-48)
Product Details
What is NDC 72663-205?
What are the uses for Welly Travel Medicine Kit?
Which are Welly Travel Medicine Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- MECLIZINE HYDROCHLORIDE (UNII: HDP7W44CIO)
- MECLIZINE (UNII: 3L5TQ84570) (Active Moiety)
- IBUPROFEN (UNII: WK2XYI10QM)
- IBUPROFEN (UNII: WK2XYI10QM) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- LOPERAMIDE HYDROCHLORIDE (UNII: 77TI35393C)
- LOPERAMIDE (UNII: 6X9OC3H4II) (Active Moiety)
- DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2)
- DOXYLAMINE (UNII: 95QB77JKPL) (Active Moiety)
Which are Welly Travel Medicine 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- D&C RED NO. 27 ALUMINUM LAKE (UNII: ZK64F7XSTX)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SORBITOL (UNII: 506T60A25R)
- TALC (UNII: 7SEV7J4R1U)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
- FD&C BLUE NO. 1 ALUMINUM LAKE (UNII: J9EQA3S2JM)
What is the NDC to RxNorm Crosswalk for Welly Travel Medicine Kit?
- RxCUI: 1101446 - doxylamine succinate 25 MG Oral Tablet
- RxCUI: 310965 - ibuprofen 200 MG Oral Tablet
- RxCUI: 310965 - ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral Tablet
- RxCUI: 314221 - simethicone 125 MG Chewable Tablet
- RxCUI: 978010 - loperamide HCl 2 MG Oral Tablet
* 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".