NDC 82198-0003 Sc Herbal Pain Relieving

Menthol, Methyl Salicylate

NDC Product Code 82198-0003

NDC CODE: 82198-0003

Proprietary Name: Sc Herbal Pain Relieving 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.

Non-Proprietary Name: Menthol, Methyl Salicylate What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Product Characteristics

GREEN (C48329)
Shape: RECTANGLE (C48347)

NDC Code Structure

  • 82198 - Big 5 Nutrition Llc

NDC 82198-0003-1

Package Description: 3 PATCH in 1 BAG > 2.3 g in 1 PATCH

NDC Product Information

Sc Herbal Pain Relieving with NDC 82198-0003 is a a human over the counter drug product labeled by Big 5 Nutrition Llc. The generic name of Sc Herbal Pain Relieving is menthol, methyl salicylate. The product's dosage form is patch and is administered via topical form.

Dosage Form: Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.

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 Herbal Pain Relieving 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.

  • FD&C BLUE NO. 2 (UNII: L06K8R7DQK)

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: Big 5 Nutrition Llc
Labeler Code: 82198
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: 10-11-2021 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.

Sc Herbal Pain Relieving 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

External analgesic

Otc - Active Ingredient

Active IngredientsPurposeMenthol 4%External AnalgesicMethyl Salicylate 1 %External Analgesic


For the temporary relief of minor aches and pains of muscles and joints associated with: ■ arthritis ■ strains ■ bruises ■ sprains■ simple backache


For external use only

Do Not Use

■on wounds ■ irritated or damaged skin ■ sensitive skin ■ with a heating pad ■ if pregnant ■ with, or as the same time as, other external analgesic products ■ if allergic to aspirin or salicylates ■ if allergic to any ingredients of this product

When Using This Product

■ avoid contact wit the eyes■ do not bandage tightly■ do not apply to wounds or damaged skin■ do not use more than 3 plasters a day■ do not use 1 hour before or after bathing

Stop Use And Ask Doctor

■ condttion worsens■ symptoms persist for more than 7 days■ symptoms clear up and occur again wtthin a few days■ excessive irritation of the skin develops■ rashes, itching or redness are present■ side effects occur.

Otc - Pregnancy Or Breast Feeding

If pregnant, ask a health professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children to avoid accidental poisoning.


In case of overdose, get medical help or contact a Poison Control Center right away.

Otc - Do Not Use

Do not use otherwise than as directed.


■ Adults and children 12 years of age and older: clean and dry affected area. Remove patch from the protective layer, apply to the affected area, rub the area with your hand to secure the patch.

■ Patch will remain effective for 8 hours.

■ Avoid using the same patch on the same area for more than 2 days.

■ Do not apply to area with excessive hair. Adhesive patch may hurt skin upon removal.

■ Wet patch with warm water before removing from skin

■ Children under 12 years of age: Do not use or consult a doctor.

Other Information

■ store unused patch in the pouch

■ store at room temperature, 20° to 25° C(68° to 77° F

Inactive Ingredients

Chinese Clematidis Root & Rhizome, Yellow wax, Momordica cochinchinensis seeds, Castor Seeds, Myrrh, Frankincense, Sesame Oil, Resin, FD&C Blue No. 2, FD&C Yellow No. 4, Zinc Oxide

* Please review the disclaimer below.