NDC 64942-1874 Vaseline

Healing Jelly

NDC Product Code 64942-1874

NDC 64942-1874-1

Package Description: 49 g in 1 JAR

NDC 64942-1874-2

Package Description: 71 g in 1 TUBE

NDC 64942-1874-3

Package Description: 106 g in 1 JAR

NDC 64942-1874-4

Package Description: 212 g in 1 JAR

NDC 64942-1874-5

Package Description: 368 g in 1 JAR

NDC Product Information

Vaseline with NDC 64942-1874 is a a human over the counter drug product labeled by Conopco Inc. D/b/a Unilever. The generic name of Vaseline is healing jelly. The product's dosage form is jelly and is administered via topical form.

Labeler Name: Conopco Inc. D/b/a Unilever

Dosage Form: Jelly - A class of gels, which are semisolid systems that consist of suspensions made up of either small inorganic particles or large organic molecules interpenetrated by a liquid--in which the structural coherent matrix contains a high portion of liquid, usually water.

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.

Vaseline 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.

  • PETROLATUM 99.96 g/100g

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.

  • WATER (UNII: 059QF0KO0R)

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.

Product Labeler Information

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

Labeler Name: Conopco Inc. D/b/a Unilever
Labeler Code: 64942
FDA Application Number: part347 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 FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. 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: 03-03-2021 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.

Vaseline 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

WHITE PETROLATUM, USP (100%)

Purpose

Skin protectant

Uses

  • Temporarily protects minorcutsscrapesburnstemporarily protects and helps relieve chapped or cracked skin and lipshelps protect from the drying effects of wind and cold weather

Warnings

  • For external use onlyWhen using this product do not get into eyes
  • See a doctor if condition last more than 7 days
  • Do not use on
  • Deep or puncture woundsanimal bitesserious burns

Otc - Keep Out Of Reach Of Children

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

Directions

Apply as needed

Inactive Ingredient

Water

Questions?

Call 1-800-457-7084

* Please review the disclaimer below.