NDC 62450-002 Attends Advanced Barrier
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62450 - Purna Pharmaceuticals Nv
- 62450-002 - Attends Advanced Barrier
Product Packages
NDC Code 62450-002-01
Package Description: 99 g in 1 PACKAGE
Product Details
What is NDC 62450-002?
What are the uses for Attends Advanced Barrier?
Which are Attends Advanced Barrier UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Attends Advanced Barrier 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- WATER (UNII: 059QF0KO0R)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
- WHITE WAX (UNII: 7G1J5DA97F)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- GLYCERIN (UNII: PDC6A3C0OX)
- CARNOSINE (UNII: 8HO6PVN24W)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- PANTHENOL (UNII: WV9CM0O67Z)
- MINERAL OIL (UNII: T5L8T28FGP)
- PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- TOCOPHEROL (UNII: R0ZB2556P8)
What is the NDC to RxNorm Crosswalk for Attends Advanced Barrier?
- RxCUI: 1232104 - zinc oxide 10 % Topical Spray
- RxCUI: 1232104 - zinc oxide 100 MG/ML Topical Spray
- RxCUI: 1232104 - ZNO 100 MG/ML Topical Spray
* 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".