NDC 21130-337 Bite And Sting Relief Signature Care

NDC Product Code 21130-337

NDC CODE: 21130-337

Proprietary Name: Bite And Sting Relief Signature Care 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

  • 21130 - Better Living

NDC 21130-337-03

Package Description: 85 g in 1 CAN

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

NDC Product Information

Bite And Sting Relief Signature Care with NDC 21130-337 is a product labeled by Better Living. 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: 238909.

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)
  • ASCORBIC ACID (UNII: PQ6CK8PD0R)
  • CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
  • CHAMOMILE (UNII: FGL3685T2X)
  • CHOLECALCIFEROL (UNII: 1C6V77QF41)
  • DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
  • CLOVE OIL (UNII: 578389D6D0)
  • PEPPERMINT OIL (UNII: AV092KU4JH)
  • OCTYLDODECANOL (UNII: 461N1O614Y)
  • OLIVE OIL (UNII: 6UYK2W1W1E)
  • PEG-8 DIMETHICONE (UNII: GIA7T764OD)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
  • VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
  • ALCOHOL (UNII: 3K9958V90M)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA (UNII: 208G222332)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • CORN OIL (UNII: 8470G57WFM)

Product Labeler Information

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

Labeler Name: Better Living
Labeler Code: 21130
Start Marketing Date: 03-30-2018 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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Bite And Sting Relief Signature Care Product Label Images

Bite And Sting Relief Signature Care 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

Uses

For the temporary relief of pain and itching associated with insect bites.

Inactive Ingredients

Aloe Barbadensis Leaf ExtractAscorbic AcidCamphorChamomilla Recutita (Matricaria) Flower ExtractCholecalciferolDiisopropyl AdipateEugenia Caryophyllus (Clove) Flower OilFragranceMentha Piperita (Peppermint) OilOctyldodecanolOlea Europaea (Olive) Fruit OilPEG-8 DimethiconePropylene GlycolPyridoxine HClRetinyl PalmitateSD Alcohol 40SilicaSodium Propoxyhydroxypropyl Thiosulfate SilicaTocopheryl AcetateZea Mays (Corn) Oil

* Please review the disclaimer below.