NDC 61767-222 Zinc Oxide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61767 - Blossom Pharmaceuticals
- 61767-222 - Zinc Oxide
Product Packages
NDC Code 61767-222-01
Package Description: 72 TUBE in 1 CASE / 56.68 g in 1 TUBE
NDC Code 61767-222-02
Package Description: 12 JAR in 1 CASE / 425.1 g in 1 JAR
NDC Code 61767-222-03
Package Description: 72 TUBE in 1 CASE / 28.34 g in 1 TUBE
Product Details
What is NDC 61767-222?
What are the uses for Zinc Oxide?
Which are Zinc Oxide 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 Zinc Oxide 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:
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETETH-20 (UNII: I835H2IHHX)
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- PETROLATUM (UNII: 4T6H12BN9U)
What is the NDC to RxNorm Crosswalk for Zinc Oxide?
- RxCUI: 198911 - zinc oxide 20 % Topical Ointment
- RxCUI: 198911 - zinc oxide 0.2 MG/MG Topical Ointment
- RxCUI: 198911 - zinc oxide 200 MG per GM Topical Ointment
- RxCUI: 198911 - ZNO 0.2 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".