NDC 62450-001 Attends Daily Barrier
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62450 - Purna Pharmaceuticals Nv
- 62450-001 - Attends Daily Barrier
Product Packages
NDC Code 62450-001-01
Package Description: 99 g in 1 PACKAGE
Product Details
What is NDC 62450-001?
What are the uses for Attends Daily Barrier?
Which are Attends Daily Barrier UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Attends Daily 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)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CARNOSINE (UNII: 8HO6PVN24W)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- PANTHENOL (UNII: WV9CM0O67Z)
- MINERAL OIL (UNII: T5L8T28FGP)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ALMOND OIL (UNII: 66YXD4DKO9)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- TOCOPHEROL (UNII: R0ZB2556P8)
What is the NDC to RxNorm Crosswalk for Attends Daily Barrier?
- RxCUI: 1491554 - dimethicone 2 % / zinc oxide 4 % Topical Spray
- RxCUI: 1491554 - dimethicone 20 MG/ML / zinc oxide 40 MG/ML Topical Spray
- RxCUI: 1491554 - dimethicone 20 MG/ML / ZNO 40 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".