NDC 77249-105 Echo Pearl Antiseptic Hand Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77249 - Atlantic Care Chemicals Private Limited
- 77249-105 - Echo Pearl Antiseptic Hand Wash
Product Packages
NDC Code 77249-105-01
Package Description: .1 L in 1 BOTTLE
NDC Code 77249-105-02
Package Description: .2 L in 1 BOTTLE
NDC Code 77249-105-05
Package Description: .5 L in 1 BOTTLE
NDC Code 77249-105-45
Package Description: 5 L in 1 CAN
Product Details
What is NDC 77249-105?
Which are Echo Pearl Antiseptic Hand Wash UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Echo Pearl Antiseptic Hand Wash 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:
- LAURYL ALCOHOL (UNII: 178A96NLP2)
- S-METHYL METHANETHIOSULFONATE (UNII: 0906Z2356U)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- WATER (UNII: 059QF0KO0R)
- BOROGLYCERIN (UNII: U3LMU4AN21)
- CLOVE OIL (UNII: 578389D6D0)
What is the NDC to RxNorm Crosswalk for Echo Pearl Antiseptic Hand Wash?
- RxCUI: 1439778 - benzalkonium chloride 0.2 % Medicated Liquid Soap
- RxCUI: 1439778 - benzalkonium chloride 2 MG/ML Medicated Liquid Soap
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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".