NDC 11822-1236 First Aid Sensitive Anti-itch

NDC Product Code 11822-1236

NDC 11822-1236-6

Package Description: 222 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

First Aid Sensitive Anti-itch with NDC 11822-1236 is a product labeled by Rite Aid. The generic name of First Aid Sensitive Anti-itch is . The product's dosage form is and is administered via form.

Labeler Name: Rite Aid

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

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.

  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • CHAMOMILE (UNII: FGL3685T2X)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
  • PEG-100 STEARATE (UNII: YD01N1999R)
  • PEG-8 STEARATE (UNII: 2P9L47VI5E)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

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

Labeler Name: Rite Aid
Labeler Code: 11822
Start Marketing Date: 12-31-2012 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 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. Values = ‘Y’ or ‘N’.

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Information for Patients

Pramoxine

Pramoxine is pronounced as (pra mox' een)

Why is pramoxine medication prescribed?
Pramoxine is used to temporarily relieve pain and itching from insect bites; poison ivy, poison oak, or poison sumac; minor cuts, scrapes, or burns; minor skin irritation...
[Read More]

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First Aid Sensitive Anti-itch Product Label Images

First Aid Sensitive Anti-itch 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

Inactive Ingredients

Aloe Barbadensis Leaf JuiceCarbomerCetyl AlcoholChamomilla Recutita (Matricaria) Flower ExtractEthylhexylglycerinGlyceryl StearateIsopropyl MyristatePEG-100 StearatePEG-8 StearatePetrolatumPhenoxyethanolSodium HydroxideStearic AcidWater

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