NDC 59672-0732 Trip Ease

NDC Product Code 59672-0732

NDC 59672-0732-2

Package Description: 32 TABLET in 1 BLISTER PACK

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

NDC Product Information

Trip Ease with NDC 59672-0732 is a product labeled by Lc Industries. The generic name of Trip Ease is . The product's dosage form is and is administered via form.

Labeler Name: Lc Industries

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.

  • DEXTROSE (UNII: IY9XDZ35W2)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Labeler Information

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

Labeler Name: Lc Industries
Labeler Code: 59672
Start Marketing Date: 05-04-2012 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’.

* Please review the disclaimer below.

Trip Ease 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

Otc - Purpose

Active IngredientsPurposeThe letters HPUS indicate that these ingredients are officially included in the Homeopathic Pharmacopeia of the United States.Borax30C HPUSTo reduce motion sicknessCocculus Indicus30C HPUSGelsemium30C HPUSKressotum30C HPUSRhus Toxicodendron30C HPUSTabacum30C HPUS

Uses

For the relief of motion sickness associated with traveling

Otc - Do Not Use

Do not use if the blister pack is broken.

Otc - Ask Doctor

Ask a doctor before use in children under 2 years of age.

Otc - Stop Use

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen.

Otc - Pregnancy Or Breast Feeding

If pregnant or breast-feeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Directions

AgeDoseAdults and Children 2 years and overChew one tablet at start of trip, and one tablet every hour while problem persists. However variation of these directions is acceptable and may be preferable. Best if taken 1 hour before and after meals.Under 2 yearsAsk a doctor.

Other Information

  • Store under 86°F (30°C)No drug interactionsNon-drowsy

Inactive Ingredients

Dextrose and separating agents magnesium stearate and silicon dioxide.

Other

Distributed to retailers byL.C. Industries, IncElk Grove Village, IL 60007

* Please review the disclaimer below.