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Wegmans aloe after sun gel with lidocaine hcl external analgesic - Medication Information

Product NDC Code 47124-129
Drug Name

Wegmans aloe after sun gel with lidocaine hcl external analgesic

Type Brand
Pharm Class Amide Local Anesthetic [EPC],
Amides [CS],
Antiarrhythmic [EPC],
Local Anesthesia [PE]
Active Ingredients
Lidocaine hydrochloride 8 mg/g
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 1098616
Application Number part348
Labeler Name WEGMANS FOOD MARKETS INC
Packages
Package NDC Code Description
47124-129-68 454 g in 1 bottle (47124-129-68)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Lidocaine 0.8% (as Lidocaine HCI)

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 • Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily • Children under 2 years of age: Ask a doctor.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients water, aloe barbadensis leaf juice, SD alcohol 40-B, laureth-23, polysorbate 20, glycerin, allantoin, carbomer, triethanolamine, menthyl lactate, menthol, fragrance, aleurites moluccanus seed extract, carica papaya (papaya) fruit extract, colocasia antiquorum root extract, mangifera indica (mango) fruit extract, passiflora incarnata flower extract, plumeria acutifolia flower extract, psidium guajava fruit extract, tocopheryl acetate (vitamin E acetate), tocopherol, phenoxyethanol, benzyl alcohol, 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 relief of pain and itching associated with sunburn, minor burns, minor cuts, scrapes, insect bites, and minor skin irritations

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Wegmans Aloe After Sun Gel with Lidocaine HCl External Analgesic Lidocaine Hydrochloride PHENOXYETHANOL BENZYL ALCOHOL MANGO ALCOHOL LAURETH-23 GLYCERIN POLYSORBATE 20 ALLANTOIN CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) TROLAMINE MENTHYL LACTATE, (-)- LEVOMENTHOL KUKUI NUT OIL PAPAYA COLOCASIA ESCULENTA ROOT PASSIFLORA INCARNATA FLOWER GUAVA .ALPHA.-TOCOPHEROL ACETATE .ALPHA.-TOCOPHEROL, DL- ALOE VERA LEAF WATER PLUMERIA ALBA FLOWER OIL LIDOCAINE HYDROCHLORIDE LIDOCAINE LIDOCAINE HYDROCHLORIDE ANHYDROUS

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 WEG47651E3

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 large quantities, particularly over raw surfaces or blistered areas

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, seek medical help or contact a Poison Control Center immediately.

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 persist for more than 7 days • symptoms clear up and occur again within 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 avoid contact with eyes. If contact occurs, 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.
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