NDC 68233-806 Sc Pain Relief Balm

Methyl Salicylate, Menthol, Camphor

NDC Product Code 68233-806

NDC 68233-806-01

Package Description: 1 JAR in 1 BOX > 35 g in 1 JAR

NDC Product Information

Sc Pain Relief Balm with NDC 68233-806 is a a human over the counter drug product labeled by Albert Max, Inc.. The generic name of Sc Pain Relief Balm is methyl salicylate, menthol, camphor. The product's dosage form is ointment and is administered via topical form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1990875.

Dosage Form: Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

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.

Sc Pain Relief Balm 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.

  • EUCALYPTUS OIL (UNII: 2R04ONI662)
  • LAVENDER OIL (UNII: ZBP1YXW0H8)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • WHITE WAX (UNII: 7G1J5DA97F)

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: Albert Max, Inc.
Labeler Code: 68233
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: 09-01-2006 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: 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.

Sc Pain Relief Balm Product Label Images

Sc Pain Relief Balm 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 20.7%Menthol 15.6%Camphor 3.1%

​Purpose

External Analgesic

​Uses

For the temporary relief of minor aches and pains of muscles and joints due to:• arthritis • ​strains ​• bruises ​• ​sprains ​•​ simple backache

​Warnings

  • For external use only.Do not useon wounds • irritated or damaged skinsensitive skin • with a heating pad • if pregnantwith, or as the same time as, other external analgesic productsif allergic to aspirin or salicylatesif allergic to any ingredients of this productWhen using this productavoid contact with the eyesdo not bandage tightlydo not apply to wounds or damaged skindo not use 1 hour before or after bathingStop use and ask a doctor ifcondition worsens symptoms persist for more than 7 days symptoms clear up and occur again within a few days excessive irritation of the skin developsredness is present  • side effects occur.If pregnant, ask a health professional before use.

Directions

  • ​Apply to the affected area. Rub well on affected area.Repeat 2 times daily.​​Children under 2 years of age: Do not use or consult a doctor

Other Information

  • Store at room temperature, 20 to 25​o​C(68 to 77​o​F)​​​

Inactive Ingredients

Eucalyptus oil, Lavender oil, Vaseline, White beeswax

* Please review the disclaimer below.