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White rain cocoa butter petroleum jelly - Medication Information

Product NDC Code 52862-133
Drug Name

White rain cocoa butter petroleum jelly

Type Brand
Active Ingredients
Petrolatum 99.9 g/100g
Route TOPICAL
Dosage Form JELLY
RxCUI drug identifier 1148414
Application Number part347
Labeler Name INTERNATIONAL WHOLESALE INC.
Packages
Package NDC Code Description
52862-133-01 170 g in 1 jar (52862-133-01)
52862-133-03 50 g in 1 jar (52862-133-03)
52862-133-04 113 g in 1 jar (52862-133-04)
52862-133-05 226 g in 1 jar (52862-133-05)
52862-133-06 283 g in 1 jar (52862-133-06)
52862-133-07 100 g in 1 jar (52862-133-07)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient White Petrolatum USP (99%)

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 apply product liberally, as often as necessary.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Theobroma Cacao (Cocoa) Seed Butter, fragrance

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 • For the temporary protection of minor cuts, scrapes, burns • Helps to temporarily protect chafed, chapped, cracked or windburned skin and lips.

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.
white rain Cocoa Butter Petroleum Jelly 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.
Label

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 wounds, animal bites, or serious burns. Ask a doctor.

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 doctor if condition worsens or does not improve within 7 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 avoid contact with 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