NDC 69264-014 Callus Removal Foot Pack
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69264 - Polaroisin International Co., Ltd.
- 69264-014 - Callus Removal Foot Pack
Product Packages
NDC Code 69264-014-25
Package Description: 2 PATCH in 1 BAG
Product Details
What is NDC 69264-014?
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:
- LACTIC ACID (UNII: 33X04XA5AT)
- WATER (UNII: 059QF0KO0R)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- XANTHAN GUM (UNII: TTV12P4NEE)
- COLLAGEN ALPHA-1(III) (HUMAN) (UNII: 5D8UAE62VB)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- MANDELIC ACID (UNII: NH496X0UJX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CUCUMBER (UNII: YY7C30VXJT)
- METHYL GLUCETH-20 (UNII: J3QD0LD11P)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- UREA (UNII: 8W8T17847W)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TREHALOSE (UNII: B8WCK70T7I)
What is the NDC to RxNorm Crosswalk for Callus Removal Foot Pack?
- RxCUI: 1594682 - salicylic acid 0.19 % Topical Patch
- RxCUI: 1594682 - salicylic acid 1.9 MG/ML Medicated Pad
- RxCUI: 1594682 - salicylic acid 0.19 % Medicated Pad
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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".