NDC 69693-416 Absorbine Jr. Plus Knee

Camphor, Menthol

NDC Product Code 69693-416

NDC 69693-416-00

Package Description: 1 PATCH in 1 POUCH > 38.22 mg in 1 PATCH

NDC 69693-416-01

Package Description: 6 POUCH in 1 CARTON > 1 PATCH in 1 POUCH > 38.22 mg in 1 PATCH

NDC 69693-416-02

Package Description: 18 POUCH in 1 CARTON > 1 PATCH in 1 POUCH > 38.22 mg in 1 PATCH

NDC Product Information

Absorbine Jr. Plus Knee with NDC 69693-416 is a a human over the counter drug product labeled by Clarion Brands, Llc. The generic name of Absorbine Jr. Plus Knee is camphor, menthol. The product's dosage form is patch and is administered via topical form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 2584850.

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.

Absorbine Jr. Plus Knee 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.

  • CLOVE OIL (UNII: 578389D6D0)

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: Clarion Brands, Llc
Labeler Code: 69693
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: 01-01-2022 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.

Absorbine Jr. Plus Knee Product Label Images

Absorbine Jr. Plus Knee 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

Active IngredientPurposeCamphor 7.0%Topical AnalgesicMenthol 7.0%Topical Analgesic

Indications & Usage

  • Uses temporarily relieves minor pain associated with:arthritismuscle strainssprainsbruisesjoint pain


For external use only

When Using This Product

  • Use only as directed do not bandage tightly or use with a heating pad avoid contact with eyes and mucous membranesdo not apply to wounds or damaged, broken or irritated skindo not use at the same time as other topical analgesics

Stop Use And Ask A Doctor If

  • Condition worsens redness is present irritation developssymptoms persist for more that 7 days or clear up and occur again within a few days

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 over 12 years:clean and dry the affected arearemove backing from patch and apply patch to affected areause 1 patch for 8 to 12 hours, once a daychildren 12 years or younger: ask a doctor

Storage And Handling

Other information store at room temperature below 86ºF (30ºC)

Inactive Ingredient

Inactive ingredients adhesive plaster, eucalyptus globulus leaf oil, gaultheria fragrantissima (wintergreen) oil, clove (syzygum aromaticum) flower oil

* Please review the disclaimer below.