NDC 50145-222 Hipoglos
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 50145-222-01
Package Description: 1 TUBE in 1 CARTON / 120 g in 1 TUBE
NDC Code 50145-222-02
Package Description: 1 TUBE in 1 CARTON / 100 g in 1 TUBE
NDC Code 50145-222-03
Package Description: 1 TUBE in 1 CARTON / 72 g in 1 TUBE
NDC Code 50145-222-04
Package Description: 1 TUBE in 1 CARTON / 60 g in 1 TUBE
NDC Code 50145-222-05
Package Description: 1 TUBE in 1 CARTON / 5 g in 1 TUBE
Product Details
What is NDC 50145-222?
What are the uses for Hipoglos?
Which are Hipoglos UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- LANOLIN (UNII: 7EV65EAW6H)
- LANOLIN (UNII: 7EV65EAW6H) (Active Moiety)
Which are Hipoglos 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:
- ALCOHOL (UNII: 3K9958V90M)
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- COD LIVER OIL (UNII: BBL281NWFG)
- ENGLISH LAVENDER OIL (UNII: ZBP1YXW0H8)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- TALC (UNII: 7SEV7J4R1U)
- VANILLIN (UNII: CHI530446X)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Hipoglos?
- RxCUI: 1249131 - lanolin 15 % / zinc oxide 15 % Topical Ointment
- RxCUI: 1249131 - lanolin 0.15 MG/MG / zinc oxide 0.15 MG/MG Topical Ointment
- RxCUI: 1249131 - Lanolin 0.15 MG/MG / ZNO 0.15 MG/MG Topical Ointment
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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".