NDC 73076-133 Wound Care
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73076 - Shenzhen Ishan Technology Co.,ltd
- 73076-133 - Wound Care
Product Packages
NDC Code 73076-133-01
Package Description: 25 g in 1 BOTTLE
NDC Code 73076-133-02
Package Description: 50 g in 1 BOTTLE
NDC Code 73076-133-03
Package Description: 100 g in 1 BOTTLE
NDC Code 73076-133-04
Package Description: 15 g in 1 BOTTLE
Product Details
What is NDC 73076-133?
What are the uses for Wound Care?
Which are Wound Care 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 Wound Care 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:
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- SESAME OIL (UNII: QX10HYY4QV)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
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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".