NDC 63691-027 Signature Home Ab Orange

NDC Product Code 63691-027

NDC 63691-027-10

Package Description: 709 mL in 1 BOTTLE

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

NDC Product Information

Signature Home Ab Orange with NDC 63691-027 is a product labeled by Sun Products Corporation. The generic name of Signature Home Ab Orange is . The product's dosage form is and is administered via form.

Labeler Name: Sun Products Corporation

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.

  • SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
  • SODIUM LAURYL SULFATE (UNII: 368GB5141J)
  • SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
  • ALCOHOL (UNII: 3K9958V90M)
  • EDETATE SODIUM (UNII: MP1J8420LU)
  • METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • D&C RED NO. 33 (UNII: 9DBA0SBB0L)
  • WATER (UNII: 059QF0KO0R)
  • BENZISOTHIAZOLINONE (UNII: HRA0F1A4R3)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
  • SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)

Product Labeler Information

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

Labeler Name: Sun Products Corporation
Labeler Code: 63691
Start Marketing Date: 04-30-2016 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: 12-31-2018 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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Signature Home Ab Orange Product Label Images

Signature Home Ab Orange 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

Dishwashing Liquid & Antibacterial Hand Soap

ULTRA Concentratedorange scent

Active Ingredient

Chloroxylenol 0.30%

Purpose

Antibacterial hand soap

Use

For handwashing to decrease bacteria on the skin

Warnings

For external use only.

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

Wet hands and forearms. Apply 5 ml or palmful to hands and forearms. Scrub thoroughly for 30 sec. and rinse.

Inactive Ingredients

Water, Sodium Laureth Sulfate, Sodium Didecylbenzenesulfonate, Sodium Chloride, Alcohol Denat., Sodium Xylenesulfonate, Sodium Lauryl Sulfate, Tetrasodium EDTA, Benzisothiazolinone, Methylisothiazolinone, Methylchloroisothiazolinone, Fragrance, FD&C Yello No. 5, D&C Red No. 33

Questions?

Questions? 1-888-723-3929

* Please review the disclaimer below.