NDC 69540-0018 Clorox Oxi Dish Oxi Magic

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  3. NDC: 69540-0018 Clorox Oxi Dish Oxi Magic

NDC Product Code 69540-0018

NDC CODE: 69540-0018

Proprietary Name: Clorox Oxi Dish Oxi Magic 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.

Product Characteristics

Color(s):
BLUE (C48333)

NDC Code Structure

  • 69540 - Brand Buzz

NDC 69540-0018-1

Package Description: 768.912 mL in 1 BOTTLE, DISPENSING

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

NDC Product Information

Clorox Oxi Dish Oxi Magic with NDC 69540-0018 is a product labeled by Brand Buzz. The product's dosage form is and is administered via form.

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)
  • SODIUM LAURYL SULFATE (UNII: 368GB5141J)
  • SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
  • LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
  • SODIUM BICARBONATE (UNII: 8MDF5V39QO)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)
  • BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
  • LINALOOL, (+/-)- (UNII: D81QY6I88E)

Product Labeler Information

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

Labeler Name: Brand Buzz
Labeler Code: 69540
Start Marketing Date: 02-01-2015 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: 12-31-2017 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".

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Clorox Oxi Dish Oxi Magic Product Label Images

Clorox Oxi Dish Oxi Magic 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

Other

Drug Facts

Distributed by Brand Buzz LLC1400 Broadway, New York, NY 10018

Active Ingredient

Chloroxylenol 0.30%

Purpose

Antibacterial hand soap

Uses

  • Helps to decrease bacteria on the skin

Warnings

For external use only.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water.

Directions

  • Squeeze a small amount onto wet sponge, scrub thoroughly for 30 sec. and rinse.

Inactive Ingredients

WATER (AQUA, EAU), SODIUM LAURYL SULFATE, SODIUM LAURETH SULFATE, LAURAMINE OXIDE, SODIUM BICARBONATE, PROPYLENE GLYCOL, SODIUM CHLORIDE, CITRIC ACID, SODIUM HYDROXIDE, METHYLISOTHIAZOLINONE, DISODIUM EDTA, FRAGRANCE (PARFUM), BLUE 1 (CI 42090), EXT. VIOLET 2 (CI 60730), BUTYLPHENYL METHYLPROPIONAL, LINALOOL.

Questions?

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* Please review the disclaimer below.