NDC 61333-211 Lights Sting Relief Prep Pad
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61333 - Lights Medical Manufacture Co., Ltd.
- 61333-211 - Lights Sting Relief Prep Pad
Product Packages
NDC Code 61333-211-01
Package Description: 100 PATCH in 1 BOX / .4 g in 1 PATCH
Product Details
What is NDC 61333-211?
What are the uses for Lights Sting Relief Prep Pad?
Which are Lights Sting Relief Prep Pad UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are Lights Sting Relief Prep Pad 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)
What is the NDC to RxNorm Crosswalk for Lights Sting Relief Prep Pad?
- RxCUI: 2197238 - benzocaine 10 % Medicated Pad
- RxCUI: 2197238 - benzocaine 100 MG/ML 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".