Hydrocortisone Ointment
Product Images NDC 0168-0146

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Hydrocortisone (NDC 0168-0146). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by E. Fougera & Co. A Division Of Fougera Pharmaceuticals, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Structural Formula (Image 01)

Structural Formula (Image 01)
This text provides the molecular formula and molecular weight of a compound that contains calcium, silver, and oxygen. However, more specific information about the compound is not available.*
FDA Label Image

Principaldisplaypanel-1ozcontainer (Image 02)

Principaldisplaypanel-1ozcontainer (Image 02)
Hydrocortisone Ointment USP, 2.5% is a topical medication for dermatological use only, not for ophthalmic use, usually applied 2 to 4 times a day. Each gram of the medication contains 25 mg hydrocortisone with white petrolatum and mineral oil as a base. The net weight of the package is 28.35 g (1 Oz). The medication should be stored at room temperature between 15° to 30°C (59° to 86°F). To open the medication, use the cap to puncture the seal. It is important not to use the medication if the seal has been punctured or is not visible. The tube crimp mentions the medication's Lot No. and Expiration Date. E.Fougera & Co., a division of Fougera Pharmaceuticals Inc., Manufactured the medication in Meslville, New York 11747. Keep the medication out of children's reach.*
FDA Label Image

Principaldisplaypanel-1ozcarton (Image 03)

Principaldisplaypanel-1ozcarton (Image 03)
Hydrocortisone Ointment USP, 2.5% is a dermatological use only cream that shouldn't be used for ophthalmic use. The product is by the brand Fougera and it is advised to only use it 2 to 4 times a day as per the complete dosage information on the package insert. The cream should be stored at controlled room temperature between 15° to 30°C (59° to 86°F) and kept away from the reach of children. It is important to check the Control No. and Exp. Date on the crimp of the tube before using. The tube should not be used if the metal tamper-resistant seal is punctured or not visible. Each gram of the cream contains hydrocortisone in white petrolatum and mineral o base. The product net weight is 28.35 g (1 Oz).*
FDA Label Image

Principaldisplaypanel-30gcontainer (Image 04)

Principaldisplaypanel-30gcontainer (Image 04)
Hydrocortisone Cream USP, 2.5% is a dermatological use cream that should not be used for ophthalmic purposes. The usual dosage is 2 to 4 applications daily. The cream contains 25 mg of hydrocortisone and other ingredients which are listed in the insert. The cream should be stored at a controlled room temperature of 15° to 30°C (59° to 86°F) and kept out of reach of children. The tube has a net weight of 30 grams and includes Lot No. and Expiration Date. To open the tube, use the cap to puncture the seal, and do not use if the seal has been punctured or is not visible. The manufacturer is E. Fougera & Co., a division of Fougera Pharmaceuticals Inc., located in Melville, New York 11747.*
FDA Label Image

Principaldisplaypanel-30gmcarton (Image 05)

Principaldisplaypanel-30gmcarton (Image 05)
This is a description of a medication tube labeled NDC 0168-0080-31. It contains hydrocortisone cream with 2.5% strength, in a 30 gram tube. The medication is for dermatological use only and should not be used for ophthalmic purposes. The recommended dosage is 2 to 4 applications daily, and complete dosage information is included in the package insert. The medication should be stored at a controlled room temperature between 15° to 30°C (59° to 86°F), out of the reach of children. The opening of the tube has a metal tamper-resistant seal and should not be used if it is punctured or not visible. The medication is made by E. Fougera & Co., a division of Fougera Pharmaceuticals Inc., in Melville, New York 11747. A list of the active ingredients can be found on the tube, and crimp of tube contains the control number and expiration date.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.