NDC 75974-200 Neverpain

Product Information

Neverpain is product labeled by Anc Amazon Natural Corp.. The product's dosage form is and is administered via form.

Product Code75974-200
Proprietary Name 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.
Neverpain
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Anc Amazon Natural Corp.
Labeler Code75974
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
08-11-2016
Listing Expiration Date 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.
12-31-2018
Exclude Flag 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".
I
NDC Code Structure

What are the uses for Neverpain?


Product Packages

NDC 75974-200-01

Package Description: 29.5 mL in 1 BOTTLE, SPRAY

NDC 75974-200-03

Package Description: 8 mL in 1 BOTTLE, SPRAY

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

Product Details

What are Neverpain Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
  • MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
  • MENTHOL (UNII: L7T10EIP3A) (Active Moiety)

NDC to RxNorm Crosswalk

What is RxNorm? RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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.
  • ALCOHOL (UNII: 3K9958V90M)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
  • COPAIFERA OFFICINALIS RESIN (UNII: 1VH544O5AT)
  • EUCALYPTUS GUM (UNII: 72T9EZC2VX)
  • PASSIFLORA INCARNATA FLOWER (UNII: K8F3G29S6Z)
  • PEPPERMINT (UNII: V95R5KMY2B)

* Please review the disclaimer below.

Neverpain Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Other



ANC NEVERPAIN

FOR EXTERNAL USE ONLY

Neverpain is a natural, deep penetrating, fast acting pain reliever free of suspected carcinogens and coloring agents. It is a nutrient in bone and muscle tissue.

Neverpain is for the temporary relief of minor aches and pains of muscles and joints associated with: simple backache, arthritis, strains, bruises and sprains.

Drug Facts

Do not contain steroids

NDC: 75974-200-01 & 75974-200-03

MADE IN USA BY

ANC Amazon Natural Corp.
265 W. 37th St., Suite 307-A
New York, NY 10018

www.neverpain.com


Otc - Active Ingredient



Active Ingredient

Menthol 5%


Otc - Purpose



Purpose

Topical Analgesic


Indications & Usage



Uses

For the temporary relief of minor aches and pains of muscles and joints associated with:

▪ simple backache

▪ arthritis

▪ strains

▪ bruises

▪ sprains


Warnings



Warnings
For external use only.

Avoid contact with the eyes.


Storage And Handling



Flammable, keep away from fire or flame.


Otc - When Using



When using this product

▪ do not apply to wounds or damaged skin
▪ do not bandage tightly


Otc - Stop Use



Stop use and ask a doctor if

  • condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.
  •  redness is present.
  •  excessive irritation of the skin develops.

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
If swallowed, get medical help or contact a Poison Control Center right away


Dosage & Administration



Directions

  • Adults and children 2 years of age and older. Apply to the affected area not more than 3 to 4 times daily.
  •  Children under 2 years of age: Consult a physician.

Inactive Ingredient



Inactive ingredients
Alcohol, aloe vera extract, camphor, copaiba, natural eucalyptus, natural passionflower and peppermint,


Otc - Questions



Questions?
Contact (212) 354-9702,
(M-F 10:00 am - 5:00 pm)


Package Label.Principal Display Panel



EXTRA STRENGTH

EXTERNAL ANALGESIC

NEVERPAIN

SPRAY


* Please review the disclaimer below.