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Dabur - Medication Information

Product NDC Code 68747-3020
Drug Name

Dabur

Type Brand
Active Ingredients
Petrolatum 100 g/100g
Route TOPICAL
Dosage Form OINTMENT
RxCUI drug identifier 204754
Application Number M016
Labeler Name Dabur India Limited
Packages
Package NDC Code Description
68747-3020-2 5 g in 1 packet (68747-3020-2)
68747-3020-3 57 g in 1 tube (68747-3020-3)
68747-3020-4 113 g in 1 tube (68747-3020-4)
68747-3020-5 425 g in 1 jar (68747-3020-5)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient White Petroleum Jelly USP [100% w/w]

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions ■ change wet and soiled diapers promptly ■ cleanse the diaper area and allow to dry ■ apply as needed

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredient None

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses ■ helps treat and prevent diaper rash ■ helps seal out wetness ■ temporarily protects minor ■ cuts ■ scrapes ■ burns ■ temporarily helps protect and relieve chapped and cracked skin or lips ■ helps prevent and protect chafed skin or minor skin irritations associated with diaper rash ■ with each diaper change, espicially at bedtime when exposure to wet diapers may be prolonged

Purpose

Information about the drug product’s indications for use.
Purpose Skin Protectant

Spl product data elements

Usually a list of ingredients in a drug product.
DABUR White Petrolatum WATER PETROLATUM PETROLATUM

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Package Label Principal Display and Drug Fact Panel

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Other Information ■ store at 59-86F (15-30C) ■ avoid excessive heat

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use on ■ deep puncture woulnd ■ animal bites ■ serious burns

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if ■ condition worsens ■ symptoms last more than 7 days or clear up and occur again in a few days

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product ■ do not get into eyes

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings For external use only

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API