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Nyu langone health lip balm - Medication Information

Product NDC Code 74458-045
Drug Name

Nyu langone health lip balm

Type Brand
Active Ingredients
Zinc oxide .2 g/100g
Route TOPICAL
Dosage Form LIPSTICK
Application Number M020
Labeler Name Guangzhou Yilong Cosmetics Co., Ltd
Packages
Package NDC Code Description
74458-045-01 5 g in 1 tube (74458-045-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredients Zinc Oxide 0.2%

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.
Dosage Squeeze out an appropriate amount of Sunscreen lip balm and spread evenly on your lips.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients PETROLATUM:69% CERA MICROCRISTALLINA:13% BEESWAX:5% SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL:5% MINERAL OIL:4.4% BUTYROSPERMUM PARKII(SHEA) BUTTER:2% MEL:1% COCOS NUCIFERA (COCONUT) OIL:0.2% ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL:0.2%

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 prevent sunburn. If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
NYU Langone Health Lip Balm Zinc Oxide ZINC OXIDE ZINC OXIDE MINERAL OIL JOJOBA OIL SHEA BUTTER YELLOW WAX

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. lf swallowed, getmedical help or contact 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 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 wate 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.
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