NDC 71016-001 Doloran

NDC Product Code 71016-001

NDC CODE: 71016-001

Proprietary Name: Doloran 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.

Product Characteristics

Shape: ROUND (C48348)

NDC Code Structure

  • 71016 - Hector Rivera Garzon Y Compania. S. En C.

NDC 71016-001-20

Package Description: 1 BOX in 1 BOX > 20 g in 1 BOX

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

NDC Product Information

Doloran with NDC 71016-001 is a product labeled by Hector Rivera Garzon Y Compania. S. En C.. The product's dosage form is and is administered via form.

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.

  • LANOLIN (UNII: 7EV65EAW6H)
  • PARAFFIN (UNII: I9O0E3H2ZE)
  • PETROLATUM (UNII: 4T6H12BN9U)

Product Labeler Information

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

Labeler Name: Hector Rivera Garzon Y Compania. S. En C.
Labeler Code: 71016
Start Marketing Date: 10-24-2016 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: 12-31-2021 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".

* Please review the disclaimer below.

Doloran Product Label Images

Doloran 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

Active Ingredients PurposeMenthol _______________________________ 2.0% Topical AnalgesicCamphor ______________________________ 8.0% Topical AnalgesicMethyl Salicylate_________________________ 8.0% Topical Analgesic

Purpose

Topical Analgesic

Use

  • Temporarily relieves the minor aches and pains of muscles and joints associated with:simple backachearthritisstrainsbruisessprains

Warnings

  • For external use onlyDo not use​ on wounds or damaged skin with a healing pad
  • Do not use on a child under 12 years of age with arthritis-like conditions
  • Avoid contact with the eyes. If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of htis product and consult a doctor. Do not apply to wounds or damaged skin. Do not bandage tightly

Otc - Keep Out Of Reach Of Children

Keep out of reach of children to avoid accidental ingestion.If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

  • Use only as directedAdults and children 12 years of age and older; apply to affected area not ore than 3 to 4 times dailyChildren under 12 years of age; ask a doctor

Inactive Ingredient

Inactive Ingredients (Petrolatum, anhydrous lanolin, parrafin)

* Please review the disclaimer below.