NDC 77338-306 Astonea En Shield Aloe Soft Vitamin Enriched
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77338 - Astonea Labs Private Limited
- 77338-306 - Astonea
Product Packages
NDC Code 77338-306-64
Package Description: 99.2 g in 1 TUBE
Product Details
What is NDC 77338-306?
What are the uses for Astonea En Shield Aloe Soft Vitamin Enriched?
Which are Astonea En Shield Aloe Soft Vitamin Enriched 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 Astonea En Shield Aloe Soft Vitamin Enriched 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:
- WATER (UNII: 059QF0KO0R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CETETH-20 (UNII: I835H2IHHX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- GLYCERIN (UNII: PDC6A3C0OX)
- LANOLIN (UNII: 7EV65EAW6H)
- MINERAL OIL (UNII: T5L8T28FGP)
- PARAFFIN (UNII: I9O0E3H2ZE)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- PONCEAU 4R (UNII: Z525CBK9PG)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
What is the NDC to RxNorm Crosswalk for Astonea En Shield Aloe Soft Vitamin Enriched?
- RxCUI: 1089065 - zinc oxide 3.8 % Topical Ointment
- RxCUI: 1089065 - zinc oxide 0.038 MG/MG Topical Ointment
- RxCUI: 1089065 - ZNO 0.038 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".