NDC 42255-603 Acne Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42255 - Zhejiang Greenface Housewares Co., Ltd.
- 42255-603 - Acne Wipes
Product Packages
NDC Code 42255-603-01
Package Description: 40 POUCH in 1 PACKAGE / .675 g in 1 POUCH
NDC Code 42255-603-02
Package Description: 30 POUCH in 1 PACKAGE / .675 g in 1 POUCH
Product Details
What is NDC 42255-603?
What are the uses for Acne Wipes?
Which are Acne Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Acne 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:
- CETEARYL ISONONANOATE (UNII: P5O01U99NI)
- CETEARETH-2 PHOSPHATE (UNII: 8NSU66JGZR)
- CETYL ACETATE (UNII: 4Q43814HXS)
- GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETEARETH-12 (UNII: 7V4MR24V5P)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- 2-BROMO-2-NITROETHANOL (UNII: FA22WV2B2Z)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Acne Wipes?
- RxCUI: 797885 - salicylic acid 0.5 % Medicated Pad
- RxCUI: 797885 - salicylic acid 5 MG/ML Medicated Pad
* 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".