NDC 69264-016 Callus Removal Foot Pack
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69264 - Polaroisin International Co., Ltd.
- 69264-016 - Callus Removal Foot Pack
Product Packages
NDC Code 69264-016-25
Package Description: 2 PATCH in 1 BAG
Product Details
What is NDC 69264-016?
What are the uses for Callus Removal Foot Pack?
Which are Callus Removal Foot Pack UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Callus Removal Foot Pack 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:
- WATER (UNII: 059QF0KO0R)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
- ALCOHOL (UNII: 3K9958V90M)
- OCTOXYNOL-11 (UNII: SQL994V0M6)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- UREA (UNII: 8W8T17847W)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- GLYCERIN (UNII: PDC6A3C0OX)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CUCUMBER (UNII: YY7C30VXJT)
- CHAMOMILE (UNII: FGL3685T2X)
- PELARGONIUM GRAVEOLENS FLOWERING TOP (UNII: 1P36QZP48P)
- HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
- LAVANDIN OIL (UNII: 9RES347CKG)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
* 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".