NDC 64048-7336 Bite Relief Scherer Labs

NDC Product Code 64048-7336

NDC CODE: 64048-7336

Proprietary Name: Bite Relief Scherer Labs 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

  • 64048 - Product Quest Mfg.

NDC 64048-7336-2

Package Description: 1 TUBE in 1 CARTON > 52 mL in 1 TUBE

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

NDC Product Information

Bite Relief Scherer Labs with NDC 64048-7336 is a product labeled by Product Quest Mfg.. 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: 198494.

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)
  • PEG-2 STEARATE (UNII: 94YQ11Y95F)
  • ALCOHOL (UNII: 3K9958V90M)
  • HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
  • HYDROCORTISONE (UNII: WI4X0X7BPJ)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • CHAMOMILE (UNII: FGL3685T2X)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • OLIVE OIL (UNII: 6UYK2W1W1E)
  • CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
  • MENTHOL (UNII: L7T10EIP3A)
  • PEPPERMINT (UNII: V95R5KMY2B)
  • CLOVE OIL (UNII: 578389D6D0)
  • PAPAIN (UNII: A236A06Y32)

Product Labeler Information

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

Labeler Name: Product Quest Mfg.
Labeler Code: 64048
Start Marketing Date: 02-10-2012 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".

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Information for Patients

Hydrocortisone Topical

Hydrocortisone Topical is pronounced as (hye droe kor' ti sone)

Why is hydrocortisone topical medication prescribed?
Hydrocortisone is available with or without a prescription. Low-strength preparations (0.5% or 1%) are used without a prescription for the temporary relief of (1) minor s...
[Read More]

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Bite Relief Scherer Labs Product Label Images

Bite Relief Scherer Labs 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 Ingredients                   Purpose

Benzocaine                                5.00%

Uses

For temporarily relief of pain and itching associated with insect bites

Warningfor External Use Only

When using this product avoid contact with eyes and mucous membranesStop use and ask a doctor if condition worsens• symptoms last more than 7 days or clear up and occur again within a few days

Direction

Adults and children 2 years of age and older: • apply to the affected area nor mre than 3 to 4 times daily. Children under 2 years of age: consult a doctor

Inactive Ingredients

Acrylates/Dimethicone CopolymerBHTBisabololC12-15 Alkyl BenzoateCapryloyl GlycineCaprylyl GlycolCedrus Atlantica Bark ExtractCetyl DimethiconeChlorphenesinCinnamomum Zeylanicum Bark ExtractCyclopentasiloxaneDisodium EDTAEthylhexyl StearateEthylhexylglycerinGlycerinHydrated SilicaMannanNeopentyl Glycol DiheptanoatePhenoxyethanolPolyester-7Polyester-8Portulaca Oleracea ExtractPropylene GlycolSarcosineSodium PolyacrylateSteareth-100Steareth-2Styrene/Acrylates CopolymerTrideceth-6WaterXanthan Gum

* Please review the disclaimer below.