NDC 69825-006 Laxease
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69825 - Adven Biotech Private Limited
- 69825-006 - Laxease
Product Characteristics
Product Packages
NDC Code 69825-006-02
Package Description: 1 BOTTLE in 1 BOX / 100 g in 1 BOTTLE (69825-006-01)
Product Details
What is NDC 69825-006?
What are the uses for Laxease?
Which are Laxease UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHENOLPHTHALEIN (UNII: 6QK969R2IF)
- PHENOLPHTHALEIN (UNII: 6QK969R2IF) (Active Moiety)
- SENNA LEAF (UNII: AK7JF626KX)
- SENNA LEAF (UNII: AK7JF626KX) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Laxease 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:
- LACTOSE (UNII: J2B2A4N98G)
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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".