NDC 54162-500 Hydrophor

NDC Product Code 54162-500

NDC 54162-500-01

Package Description: 454 g in 1 JAR

NDC 54162-500-02

Package Description: 100 g in 1 JAR

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

NDC Product Information

Hydrophor with NDC 54162-500 is a product labeled by Geritrex Llc. The generic name of Hydrophor is . The product's dosage form is and is administered via form.

Labeler Name: Geritrex Llc

Dosage Form: -

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.

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.


Product Labeler Information

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

Labeler Name: Geritrex Llc
Labeler Code: 54162
Start Marketing Date: 07-31-2015 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: 12-31-2019 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Hydrophor Product Label Images

Hydrophor 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

Drug Facts

Active Ingredients: Petrolatum 42%Purpose: Skin protectant


• Rehydrates dry, chapped or chafedskin.• May be used alone as a skin lubricantor protectant.


Apply generously to affected areasor as directed by your physician.

Dosage & Administration

Apply generously to affected area


For External Use Only.When using this product:• Avoid contact with eyes.• If the condition worsens,discontinue use and contact aphysician.

Inactive Ingredient

Ceresin, Lanolin Alcohol,Microcrystalline Wax, Mineral Oil,Phenoxyethanol

Storage And Handling

Store at room temperature (59°F-86°F).

Otc - Keep Out Of Reach Of Children


* Please review the disclaimer below.