NDC 27495-026 Power Pain Relief Stick

Pain Relief Stick

NDC Product Code 27495-026

NDC 27495-026-02

Package Description: 72 g in 1 JAR

NDC Product Information

Power Pain Relief Stick with NDC 27495-026 is a a human over the counter drug product labeled by Physicians Science And Nature, Inc.. The generic name of Power Pain Relief Stick is pain relief stick. The product's dosage form is stick and is administered via topical form.

Dosage Form: Stick - A dosage form prepared in a relatively long and slender often cylindrical form.

Product Type: Human Otc Drug 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.

Power Pain Relief Stick Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.


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.

  • DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
  • CANNABIDIOL (UNII: 19GBJ60SN5)
  • MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • LOW DENSITY POLYETHYLENE (UNII: J245LN42AI)
  • CERESIN (UNII: Q1LS2UJO3A)
  • TOCOPHEROL (UNII: R0ZB2556P8)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Physicians Science And Nature, Inc.
Labeler Code: 27495
FDA Application Number: part348 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 11-01-2021 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: 12-31-2022 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: N - NO 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.

Power Pain Relief Stick Product Label Images

Power Pain Relief Stick 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

Methyl Salicylate 25%Menthol 15%Capsaicin 0.025%

Purpose:

Topical Analgesic

Uses:

For temporary relief of minor aches and pains of muscles and joints associated with arthritis, simple backache, sprains and strains. Does not prevent or cure any disease.

Warnings:

For external use only. Do not use in or on the eyes, mouth, mucous membranes or genitalia. Do not allow treated skin to contact infants, children or pets. Do not tightly bandage. Do not use with a heating pad. Do not use with other topical pain-relieving medications. May result in burning sensation of the skin or skin rash. Do not drive or operate heavy machinery if drowsy while using this medication. May result in stains to clothing, bedding or furniture.

Stop Use And Ask A Physician:

For severe undiagnosed pain. If pain worsens or persists for more than 7 days. If pain clears up and then recurs in a few days. If itching or skin rash occurs. If any other adverse event occur.

Do Not Use:

On cuts, infected skin or over raw or blistered skin, on children under 12 years of age or pets, in large amounts, if allergic to any of the listed ingredients, if you are pregnant or nursing, taking anticoagulant medications. If you have questions regarding the safe use of this medication, please contact your medical provider.

Keep Out Of Reach Of Children And Pets:

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

Directions:

Consult a physician prior to use. Use only as directed. Prior to first use, rub a small amount on the forearm to check for sensitivity. Gently rub over painful areas no more than 4 times daily. Do not massage into skin vigorously. Wash hands thoroughly after each use. If place into eyes, rinse with cold water and call for medical help.

Inactive Ingredients:

Caprylic/Capric Triglyceride, Polyethylene, Ozokerite, Microcrystalline Wax, Dimethyl Sulfoxide, Tocopherol, Cannabis Sativa (Hemp) Extract (300 mg Cannabidiol), Fragrance.

Formulated By A Physician

Made in the USA Manufactured for
Physicians Science andNature, Inc. -220 Newport Center Dr., 11-634,
Newport Beach, CA 92660.For further information or to place an ordervisit:
www.OCFightDoc.com or call
714-258-7116

Kessler Family Wellness

NDC 27495-026-02POWER PAIN RELIEF STICKWITH BROAD-SPECTRUM HEMP EXTRACTDOES NOT CONTAIN THCCONTAINS 300mg CBDRecommended by Physicians2.5 ounces (72 gm)

* Please review the disclaimer below.