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

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.

  • CERESIN (UNII: Q1LS2UJO3A)
  • LANOLIN ALCOHOLS (UNII: 884C3FA9HE)
  • PARAFFIN (UNII: I9O0E3H2ZE)
  • MINERAL OIL (UNII: T5L8T28FGP)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)

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 - 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.

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

Uses

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

Directions

Apply generously to affected areasor as directed by your physician.

Dosage & Administration

Apply generously to affected area

Warnings

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

KEEP OUT OF REACH OF CHILDREN.

* Please review the disclaimer below.