NDC 70990-002 Footscriptions Foot Repair
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70990 - Donegal Bay Ltd
- 70990-002 - Footscriptions Foot Repair
Product Packages
NDC Code 70990-002-01
Package Description: 252 mL in 1 TUBE
Product Details
What is NDC 70990-002?
What are the uses for Footscriptions Foot Repair?
Which are Footscriptions Foot Repair UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Footscriptions Foot Repair 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)
- ALOE ANDONGENSIS LEAF (UNII: N1P4NU25EJ)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- MINERAL OIL (UNII: T5L8T28FGP)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- PEG-100 STEARATE (UNII: YD01N1999R)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- UREA (UNII: 8W8T17847W)
- CHONDRUS CRISPUS (UNII: OQS23HUA1X)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
What is the NDC to RxNorm Crosswalk for Footscriptions Foot Repair?
- RxCUI: 200066 - menthol 0.1 % Topical Cream
- RxCUI: 200066 - menthol 1 MG/ML Topical Cream
* 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".