NDC 11822-1240 Daylogic Antibacterial Foaming Wash
Benzalkonium Chloride Soap Topical
Product Information
What is NDC 11822-1240?
The NDC code 11822-1240 is assigned by the FDA to the product Daylogic Antibacterial Foaming Wash which is a human over the counter drug product labeled by Rite Aid Corporation. The generic name of Daylogic Antibacterial Foaming Wash is benzalkonium chloride. The product's dosage form is soap and is administered via topical form. The product is distributed in 2 packages with assigned NDC codes 11822-1240-7 222 ml in 1 bottle, plastic , 11822-1240-8 222 ml in 1 bottle, plastic . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.
What are the uses for Daylogic Antibacterial Foaming Wash?
This product is used as Antibacterial. For hand washing to decrease bacteria on the skin.
Product Packages
NDC Code 11822-1240-7
Package Description: 222 mL in 1 BOTTLE, PLASTIC
NDC Code 11822-1240-8
Package Description: 222 mL in 1 BOTTLE, PLASTIC
Product Details
What are Daylogic Antibacterial Foaming Wash Active Ingredients?
Daylogic Antibacterial Foaming Wash Active Ingredients UNII Codes
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
NDC to RxNorm Crosswalk
- RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap
Daylogic Antibacterial Foaming Wash Inactive Ingredients UNII Codes
- WATER (UNII: 059QF0KO0R)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- GLYCERIN (UNII: PDC6A3C0OX)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- HYDROXYETHYL CELLULOSE (5000 CPS AT 1%) (UNII: X70SE62ZAR)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
- EDETATE SODIUM (UNII: MP1J8420LU)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SULISOBENZONE (UNII: 1W6L629B4K)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
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Daylogic Antibacterial Foaming Wash Product Label
FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.
Product Label Table of Contents
Active Ingredient
Benzalkonium Chloride 0.13%
Purpose
Antibacterial
Uses
for hand washing to decrease bacteria on the skin.
Warnings
For external use only.
When Using This Product
avoid contact with eyes. In case of contact, rinse thoroughly with water.
Stop Use And Ask A Doctor If
irritation and redness develops and lasts
Keep Out Of Reach Of Children.
In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.
Directions
- apply onto dry hands.
- lather and rinse thoroughly.
Other Information
store at room temperature.
Inactive Ingredients
Water (Aqua), Cocamidopropyl Betaine, Polysorbate 20, Fragrance (Parfum), Glycerin, Decyl Glucoside, Hydroxyethylcellulose, Aloe Barbadensis Leaf Juice, Camellia Sinensis Leaf Extract, Polyquaternium-7, Tetrasodium EDTA, Sodium Citrate, Citric Acid, Benzophenone-4, Methylchloroisothiazolinone, Methylisothiazolinone, Red 4 (CI 14700), Yellow 5 (CI 19140).
Label Copy
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