NDC 61767-228 Dyna1199 With Dimethicone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61767 - Blossom Pharmaceuticals
- 61767-228 - Dyna1199 With Dimethicone
Product Packages
NDC Code 61767-228-01
Package Description: 5 g in 1 PACKET
NDC Code 61767-228-02
Package Description: 15 g in 1 PACKET
NDC Code 61767-228-03
Package Description: 114 g in 1 TUBE
NDC Code 61767-228-04
Package Description: 427.5 g in 1 JAR
Product Details
What is NDC 61767-228?
What are the uses for Dyna1199 With Dimethicone?
Which are Dyna1199 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 Dyna1199 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:
- LANOLIN (UNII: 7EV65EAW6H)
- CETETH-20 (UNII: I835H2IHHX)
- MINERAL OIL (UNII: T5L8T28FGP)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- VITAMIN A (UNII: 81G40H8B0T)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PETROLATUM (UNII: 4T6H12BN9U)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Dyna1199 With Dimethicone?
- RxCUI: 1591982 - dimethicone 1.8 % / zinc oxide 2 % Topical Ointment
- RxCUI: 1591982 - dimethicone 0.018 MG/MG / zinc oxide 0.02 MG/MG Topical Ointment
- RxCUI: 1591982 - dimethicone 0.018 MG/MG / ZNO 0.02 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".