NDC 69020-204 Makesense Maximum Strength

  1. Labeler Index
  2. Cherry Hill Sales Co
  3. NDC: 69020-204 Makesense Maximum Strength

NDC Product Code 69020-204

NDC CODE: 69020-204

Proprietary Name: Makesense Maximum Strength 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: 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.

NDC Code Structure

  • 69020 - Cherry Hill Sales Co

NDC 69020-204-14

Package Description: 14 g in 1 TUBE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Makesense Maximum Strength with NDC 69020-204 is a product labeled by Cherry Hill Sales Co. The generic name of Makesense Maximum Strength is . The product's dosage form is and is administered via form.

Labeler Name: Cherry Hill Sales Co

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.
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • MINERAL OIL (UNII: T5L8T28FGP)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • POLYSORBATE 60 (UNII: CAL22UVI4M)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

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

Labeler Name: Cherry Hill Sales Co
Labeler Code: 69020
Start Marketing Date: 06-15-2014 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: 12-31-2017 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Information for Patients

Hydrocortisone Topical

Hydrocortisone Topical is pronounced as (hye droe kor' ti sone)

Why is hydrocortisone topical medication prescribed?
Hydrocortisone topical is used to treat redness, swelling, itching, and discomfort of various skin conditions. Hydrocortisone is in a class of medications called corticos...
[Read More]

* Please review the disclaimer below.

Makesense Maximum Strength Product Label Images

Makesense Maximum Strength 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 Ingredient

Hydrocortisone 1%

Purpose

Anti-itch

Uses

■ for temporary relief of itching associated with minor skin irritations and rashes due to: ■ eczema  ■ seborrheic dermatitis ■ psoriasis ■insect bites ■ poison ivy, oak, sumac ■ soaps ■ detergents ■ cosmetics ■ jewelry ■  temporarily relieves external anal and genital itching   ■ other uses of this product should be under the advice and supervision of a doctor

Warnings

For external use only

Do Not Use

■ in the genital area if you have vaginal discharge. Consult a doctor ■ for the treatment of diaper rash. Consult a doctor

When Using This Product

■ avoid contact with eyes ■ do not use more than directed unless told to do so by a doctor ■ do not put directly into the rectum by using fingers or any mechanical device or applicator

Stop Use And Ask A Doctor If

■ the condition worsens, symptoms persist for more than 7 days or clear up and occur again wihin a few days, and do not beginuse of any other hydrocortisone product unless you have asked a doctor ■ rectal bleed occurs

Keep Out Of Reach Of Children

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

Directions

■


for itching of skin irritation and rashes: ■ adults and children 2 years of age and older: apply to affected


area not more than 3 to 4 times daily ■ children under 2 years of age: ask a doctor


for external anal and genital itching: adults: ■ when practical, clean the affected area with mild soap and water and rinse thoroughly        ■ gently dry by patting or blotting with toilet tissue or a soft cloth before applying ■ apply to affected area not more than 3 to 4 times daily ■ children under 12 years of age: ask a doctor

Other Information

■ store at 68-77F (20 to 25C) ■ see carton or tube crimp for lot number and expiration date

Inactive Ingredients

Cetearyl Alcohol, Disodium EDTA, Glyceryl Stearate, Methylparaben, Mineral Oil, Petrolatum, Polysorbate 60, Propylene Glycol, Propylparaben, Sorbitan Stearate, Water

* Please review the disclaimer below.