NDC 73921-017 S-oint Hydrocortisone 1%

Hydrocortisone Ointment Topical

NDC Product Code 73921-017

NDC 73921-017-30

Package Description: 1 TUBE in 1 CARTON > 30 g in 1 TUBE

NDC Product Information

S-oint Hydrocortisone 1% with NDC 73921-017 is a human over the counter drug product labeled by Global Pharma Healthcare Private Limited. The generic name of S-oint Hydrocortisone 1% is hydrocortisone. The product's dosage form is ointment and is administered via topical form.

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.

S-oint Hydrocortisone 1% 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.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates a single concept unique identifier (RXCUI) is associated with this product:

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.


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.

Pharmacologic Class(es)

What is a Pharmacological Class?
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Product Labeler Information

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

Labeler Name: Global Pharma Healthcare Private Limited
Labeler Code: 73921
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: 04-01-2021 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.

S-oint Hydrocortisone 1% Product Label Images

S-oint Hydrocortisone 1% 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 USP 1%


Steroid Cream


• For relief of itching associated with minor skin irritations and rashes due to:  • Eczema  • Insect bites  • Soaps and detergents  • Cosmetics  • Jewelry  • Seborrheic dermatitis  • Psoriasis  • Poison ivy, oak or sumac  • For external genital, feminine and anal itching  • Other uses of this product should be only under the advice and supervision of a doctor


For external use onlyDo not use  • In children under 2 years of age  • If you have a vaginal discharge  • For the treatment of diaper rashAsk a doctor before use if you have  • External genital or feminine itching  • External anal itching  • BleedingWhen using this product  • Avoid contact with eyes  • Do not exceed the recommended daily dosage unless directed by a doctor  • Do not put this product into the rectum by using fingers or any mechanical device or applicatorStop use and ask a doctor  • If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, stop use and do not begin use of any other hydrocortisone product, unless you have consulted a doctor.

Otc - Keep Out Of Reach Of Children

Keep out of the reach of children.If swallowed, get medical help or contact a Poison Control Center.


For minor skin irritations and rashes, adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily. For external anal itching:  • Adults: when practical, cleanse the affected area with mild soap and warm water and rinse thoroughly  • Gently dry by patting or blotting with toilet tissue or soft cloth before application of this product  • Children: under 12 years of age, consult a doctor.

Other Information

• Do not use if seal is damaged or is not visible. To open, unscrew cap, pull tab to remove foil seal.  • Store at room temperature  • See crimp of tube or carton for Lot Number and Expiration Date

Inactive Ingredient

Paraffin wax, Microwax, Light liquid paraffin

* Please review the disclaimer below.