NDC 69020-209 Makesense Feminine Anti-itch
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69020 - Cherry Hill Sales Co
- 69020-209 - Makesense
Product Packages
NDC Code 69020-209-21
Package Description: 21 g in 1 TUBE
Product Details
What is NDC 69020-209?
What are the uses for Makesense Feminine Anti-itch?
Which are Makesense Feminine Anti-itch UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Makesense Feminine Anti-itch 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:
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HYDROXYPROPYL BISSTEARYLDIMONIUM CHLORIDE (UNII: OVB1E9X12I)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PEG-100 STEARATE (UNII: YD01N1999R)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Makesense Feminine Anti-itch?
- RxCUI: 997658 - benzocaine 5 % / benzalkonium chloride 0.13 % Vaginal Cream
- RxCUI: 997658 - benzalkonium chloride 1.3 MG/ML / benzocaine 50 MG/ML Vaginal Cream
- RxCUI: 997658 - benzalkonium chloride 0.13 % / benzocaine 5 % Vaginal Cream
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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".