NDC 60640-2000 Lollicaine Pina Colada
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60640 - Centrix, Inc.
- 60640-2000 - Lollicaine Pina Colada
Product Characteristics
RED (C48326)
GREEN (C48329)
YELLOW (C48330)
CHERRY (C73375)
MINT (C73404)
COCONUT (C73379)
Product Packages
NDC Code 60640-2000-1
Package Description: 1 JAR in 1 CARTON / 28.35 g in 1 JAR
Product Details
What is NDC 60640-2000?
What are the uses for Lollicaine Pina Colada?
Which are Lollicaine Pina Colada UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are Lollicaine Pina Colada 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:
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
What is the NDC to RxNorm Crosswalk for Lollicaine Pina Colada?
- RxCUI: 1942189 - LolliCaine 20 % Oral Gel
- RxCUI: 1942189 - benzocaine 0.2 MG/MG Oral Gel [LolliCaine]
- RxCUI: 1942189 - LolliCaine 0.2 MG/MG Oral Gel
- RxCUI: 1942189 - LolliCaine 20 % Dental Gel
- RxCUI: 238910 - benzocaine 20 % Oral Gel
* 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".