NDC 72886-8020 Dr. Smarth Shield
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72886 - Crystal Curam
- 72886-8020 - Dr. Smarth
Product Packages
NDC Code 72886-8020-0
Package Description: 100 g in 1 TUBE
NDC Code 72886-8020-4
Package Description: 452 g in 1 JAR
Product Details
What is NDC 72886-8020?
What are the uses for Dr. Smarth Shield?
Which are Dr. Smarth Shield UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Dr. Smarth Shield 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)
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- CORN OIL (UNII: 8470G57WFM)
- LANOLIN (UNII: 7EV65EAW6H)
- MINERAL OIL (UNII: T5L8T28FGP)
- PARAFFIN (UNII: I9O0E3H2ZE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- SODIUM BORATE (UNII: 91MBZ8H3QO)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- WATER (UNII: 059QF0KO0R)
- PETROLATUM (UNII: 4T6H12BN9U)
What is the NDC to RxNorm Crosswalk for Dr. Smarth Shield?
- 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
* 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".