NDC 50382-012 Zinc Oxide And Dimethicone With Dimethicone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50382 - Galentic Pharma (india) Private Limited
- 50382-012 - Zinc Oxide And Dimethicone
Product Packages
NDC Code 50382-012-01
Package Description: 113.4 g in 1 TUBE
Product Details
What is NDC 50382-012?
What are the uses for Zinc Oxide And Dimethicone With Dimethicone?
Which are Zinc Oxide And Dimethicone With Dimethicone UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Zinc Oxide And Dimethicone With Dimethicone 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)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- LANOLIN (UNII: 7EV65EAW6H)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
- WATER (UNII: 059QF0KO0R)
- CETETH-10 (UNII: LF9X1PN3XJ)
- PARAFFIN (UNII: I9O0E3H2ZE)
- PROPYLPARABEN SODIUM (UNII: 625NNB0G9N)
- GLYCERIN (UNII: PDC6A3C0OX)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- STEARETH-20 (UNII: L0Q8IK9E08)
- POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- VITAMIN A (UNII: 81G40H8B0T)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Zinc Oxide And Dimethicone With Dimethicone?
- RxCUI: 1043605 - dimethicone 1.8 % / zinc oxide 20 % Topical Cream
- RxCUI: 1043605 - dimethicone 18 MG/ML / zinc oxide 200 MG/ML Topical Cream
- RxCUI: 1043605 - dimethicone 18 MG/ML / ZNO 200 MG/ML Topical Cream
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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".