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Vitamin a and d - Medication Information

Product NDC Code 55319-603
Drug Name

Vitamin a and d

Type Generic
Active Ingredients
Lanolin 15.5 g/100g
Petrolatum 53.4 g/100g
Route TOPICAL
Dosage Form OINTMENT
RxCUI drug identifier 664981
Application Number M016
Labeler Name MIDWOOD BRANDS, LLC
Packages
Package NDC Code Description
55319-603-01 113 g in 1 tube (55319-603-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Lanolinn - 15.5% Petrolatum - 53.4%

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 generously and massage until absorbed. Repeat as necessary.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Cod Liver Oil Fragrance Light Mineral Oil Microcrystalin Wax Water

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 temporarily protects minor cuts, scrapes and burns temporarily protects and helps relieve chapped, chafed or cracked skin and lips protects chafed skin due to diaper rash and helps seal out wetness

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.
Vitamin A and D Vitamin A and D PETROLATUM PETROLATUM MICROCRYSTALLINE WAX COD LIVER OIL FRAGRANCE 13576 LIGHT MINERAL OIL LANOLIN LANOLIN PARAFFIN

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.
PRINCIPAL DISPLAY PANEL Vitamin A&D Cream NET WT 4 OZ (113 g) 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 in eyes not for extensive burns or serious cuts, consult a physician

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 redness, irritation, swelling or pain persists or increases or if infection develops.

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