NDC 69693-411 Absorbine Jr. Plus
Menthol Liquid Topical

Product Information

Product Code69693-411
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.
Absorbine Jr. Plus
Non-Proprietary Name 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.
Menthol
Product Type 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.
Human Otc Drug
Dosage FormLiquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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.
Clarion Brands, Llc
Labeler Code69693
FDA Application Number 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.
part348
Marketing Category 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.
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
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.
06-24-2010
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.
12-31-2023
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".
N
NDC Code Structure

Usage Information


Product Packages

NDC 69693-411-04

Package Description: 1 BOTTLE, WITH APPLICATOR in 1 CARTON > 118 mL in 1 BOTTLE, WITH APPLICATOR

Product Details

Absorbine Jr. Plus is a human over the counter drug product labeled by Clarion Brands, Llc. The generic name of Absorbine Jr. Plus is menthol. The product's dosage form is liquid and is administered via topical form.


What are Absorbine Jr. Plus Active Ingredients?

The following is the list of active ingredients in this product. 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.


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.

  • ACETONE (UNII: 1364PS73AF)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • IODINE (UNII: 9679TC07X4)
  • CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
  • ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX)
  • WORMWOOD (UNII: F84709P2XV)
  • POTASSIUM IODIDE (UNII: 1C4QK22F9J)
  • THYMOL (UNII: 3J50XA376E)
  • WATER (UNII: 059QF0KO0R)
  • WORMWOOD OIL (UNII: 01756N87N8)


* Please review the disclaimer below.

Absorbine Jr. Plus 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



Active Ingredient



Menthol 4.0%


Purpose



Topical Analgesic


Uses



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

  • arthritis
  • simple backache 
  • sprains
  • strains 
  • bruises 

Warnings



For external use only. Use only as directed.

Flammable

  • Keep away from fire, flame, sparks and heated surfaces. Tighten cap firmly.

Stop Use And Ask A Doctor If



  • Condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days.

When Using This Product



  • Avoid contact with the eyes
  • Do not apply to wounds or damaged skin
  • Do not bandage tightly

If Pregnant Or Breast Feeding,



ask a health professional before use.


Keep Out Of Reach Of Children.



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


Directions



  • adults and children 2 years of age and older: apply to the affected area no more than 3 to 4 times daily
  • children under 2 years of age; consult a doctor

Inactive Ingredients



acetone, chloroxylene, FD&C blue #1, Iodine, plant extracts of calendula, echinacea, wormwood herb, potassium iodide, thymol, water, and wormwood oil


Questions?



Call 1-844-922-7672


Principal Display Panel



Extra Strength Formula

ABSORBINE jr. ® PLUS

Pain Relieving Liquid

Fast Absorbing for Rapid Relief


Relieves:
• Sore Muscles
• Arthritis Pain

No Mess Applicator Keeps Hands Clean

4 FL OZ (118 ml) 

Our fast absorbing, deep penetrating Extra Strength Formula provides even more relief to sore muscles, arthritis pain & stiffness

Fast relief from;
Sore Muscles & Cramps
Aching Joints & Stiffness
Arthritis Pain
Bruises
Sprains
Strains
Backache
Foot Pain & Discomfort

Our Extra Strength Formula is:
Fast acting
Easy to apply
Quick-drying
Non-greasy
• Non-stinging

MADE WITH PRIDE IN THE U.S.A.

Distributed by:
Clarion Brands, LLC
27070 Miles Rd., Suite A
Solon, OH 44139
1-844-922-7672    88749A
www.absorbinejr.com

Extra Strength Formula

ABSORBINE jr. ® PLUS

Pain Relieving Liquid

Fast Absorbing for Rapid Relief


Relieves:
• Sore Muscles
• Arthritis Pain

No Mess Applicator Keeps Hands Clean

4 FL OZ (118 ml) 

Our fast absorbing, deep penetrating Extra Strength formula provides even more relief to sore muscles, arthritis pain & stiffness

Fast relief from;
Sore Muscles & Cramps
Aching Joints & Stiffness
Arthritis Pain
Bruises
Sprains
Strains
Backache
Foot Pain & Discomfort

Distributed by: Clarion Brands, LLC
27070 Miles Rd., Suite A, Solon, OH 44139
1-844-922-7672     L499294110A
www.absorbinejr.com


* Please review the disclaimer below.