NDC 42255-903 Helpmate Sanitizing Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42255 - Zhejiang Greenface Housewares Co., Ltd.
- 42255-903 - Helpmate Sanitizing Wipes
Product Packages
NDC Code 42255-903-01
Package Description: 12 BAG in 1 BOX / 20 NOT APPLICABLE in 1 BAG / 3.36 g in 1 NOT APPLICABLE
NDC Code 42255-903-02
Package Description: 8 BAG in 1 BOX / 50 NOT APPLICABLE in 1 BAG / 2.81 g in 1 NOT APPLICABLE
NDC Code 42255-903-03
Package Description: 8 PACKAGE in 1 BOX / 24 BAG in 1 PACKAGE / 1 NOT APPLICABLE in 1 BAG / 2.81 g in 1 NOT APPLICABLE
NDC Code 42255-903-04
Package Description: 100 NOT APPLICABLE in 1 PAIL / 2.9 g in 1 NOT APPLICABLE
Product Details
What is NDC 42255-903?
What are the uses for Helpmate Sanitizing Wipes?
Which are Helpmate Sanitizing Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Helpmate Sanitizing Wipes 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:
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GLYCERIN (UNII: PDC6A3C0OX)
- BRONOPOL (UNII: 6PU1E16C9W)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WATER (UNII: 059QF0KO0R)
- POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
What is the NDC to RxNorm Crosswalk for Helpmate Sanitizing Wipes?
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 1.3 MG/ML Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Topical Swab
- RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Pad
- RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Swab
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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".