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Gze salicylic acidsoap - Medication Information

Product NDC Code 74458-163
Drug Name

Gze salicylic acidsoap

Type Brand
Active Ingredients
Salicylic acid 2 g/100g
Route TOPICAL
Dosage Form SOAP
RxCUI drug identifier 312882
Application Number 505G(a)(3)
Labeler Name Guangzhou Yilong Cosmetics Co., Ltd
Packages
Package NDC Code Description
74458-163-01 60 g in 1 bag (74458-163-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Salicylic Acid 2%

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.
Wet the bar and work up a creamy lather. Massage your hands over face and body,avoiding contact with eyes. Rinse well and pat dry.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Sodium Palmate Water Glycerin Sodium Chloride Prunus Armeniaca (Apricot) Seed Powder Juglans Regia (Walnut) Shell Powder Parfum Tetrasodium Etidronate Tetrasodium EDTA

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.
Wet the bar and work up a creamy lather. Massage your hands over face and body,avoiding contact with eyes. Rinse well and pat dry.

Purpose

Information about the drug product’s indications for use.
Cleanses and exfoliates the skin.

Spl product data elements

Usually a list of ingredients in a drug product.
GZE Salicylic AcidSoap Salicylic Acid 2% EDETATE SODIUM WATER SALICYLIC ACID SALICYLIC ACID ETIDRONATE TETRASODIUM PRUNUS ARMENIACA SEED JUGLANS REGIA SHELL SODIUM CHLORIDE PARFUMIDINE SODIUM PALMATE GLYCERIN

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 damaged or broken skin.

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 rash occurs.

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 keep out of eyes. Rinse with water to remove.

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.
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