NDC 63148-079 Members Selection Antibacterial

NDC Product Code 63148-079

NDC CODE: 63148-079

Proprietary Name: Members Selection Antibacterial What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

NDC 63148-079-08

Package Description: 222 mL in 1 BOTTLE, PLASTIC

NDC 63148-079-80

Package Description: 2360 mL in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Members Selection Antibacterial with NDC 63148-079 is a product labeled by Apollo Health And Beauty Care. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1233282.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
  • HYPROMELLOSES (UNII: 3NXW29V3WO)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • POLOXAMER 124 (UNII: 1S66E28KXA)
  • POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
  • EDETATE SODIUM (UNII: MP1J8420LU)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • SODIUM CITRATE (UNII: 1Q73Q2JULR)
  • METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Apollo Health And Beauty Care
Labeler Code: 63148
Start Marketing Date: 07-08-2015 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 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.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Members Selection Antibacterial Product Label Images

Members Selection Antibacterial Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient / Ingrediente Activo

Benzalkonium Chloride 0.10%

Purpose / Propósito

Antibacterial / Antibacteriano

Uses / Usos

For washing to decrease bacteria on the skin. / Para lavar y disminuir las bacterias en la piel

Warnings / Advertencias

For external use only / Solo para uso externo

When Using This Product / Al Usar Este Producto

Avoid contact with eyes. If contact occurs, rinse thoroughly with water. / evitar el contacto con los ojos. Si ocurriera, enjuagar bien con agua.

Stop Use And Ask A Doctor If / Interrumpir El Uso Y Consultar A Un Médico Si

Irritation and redness develops. / se product irritación y enrojecimiento

Keep Out Of Reach Of Children. / Mantenga Fuera Del Alcance De Los Niños.

In case of poisoning, seek medical attention and provide this package. Call the National Poison Centers / En caso de intoxicación consulte al médico y aporte esta etiqueta. Para llamar al Centro Nacional de Intoxicaciones: Panama 911; Costa Rica (506) 2223-1028, Emergency/Emergencias 911; Guatemala (502) 2251-3560; Nicaragua (505) 2289-7150; El Salvador (503) 2288-0417; Honduras (504) 2232-2322

Directions / Instrucciones

  • Apply onto wet hands / Aplicar en las manos húmedasWork into rich later and rinse off / Formar espuma y enjuagar bien

Other Information

Store at room temperature / Guardar a temperatura ambiente

Inactive Ingredients / Ingredientes Inactivos

Water (Aqua), Cocamidopropyl Betaine, Glycerin, Decyl Glucosid, Hydroxyethylcellulose, Aloe Barbadensis Leaf Juice, Fragrance (Parfum), Poloxamer 124, Polyquaternium-7, Tetrasodium EDTA, Citric Acid, Sodium Citrate, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Red 33 (CI 17200).Agua (Aqua), Cocamidopropil betaína, glicerina, decil glucósido, hidroxietil celulosa, jugo de hoja de aloe barbadensis, fragrancia (parfume), poloxamer 124, policuaternio 7, EDTA tetrasódico, ácido cítrico, citrato de sodio, meticloroisotiazolinona, metilisotiasolinona, azul (CI 42090), rojo (CI 17200)

* Please review the disclaimer below.