NDC 50302-015 Panrosa Antibacterial Hand Green Apple
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50302 - Panrosa Enterprises, Inc.
- 50302-015 - Panrosa Antibacterial Hand Green Apple
Product Packages
NDC Code 50302-015-50
Package Description: 500 mL in 1 BOTTLE
Product Details
What is NDC 50302-015?
What are the uses for Panrosa Antibacterial Hand Green Apple?
Which are Panrosa Antibacterial Hand Green Apple UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- CHLOROXYLENOL (UNII: 0F32U78V2Q) (Active Moiety)
Which are Panrosa Antibacterial Hand Green Apple 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:
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GLYCERIN (UNII: PDC6A3C0OX)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Panrosa Antibacterial Hand Green Apple?
- RxCUI: 1435989 - chloroxylenol 0.25 % Medicated Liquid Soap
- RxCUI: 1435989 - chloroxylenol 2.5 MG/ML Medicated Liquid Soap
* 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".