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Sally hansen ouch-relief wax kit - Medication Information

Product NDC Code 66184-153
Drug Name

Sally hansen ouch-relief wax kit

Type Brand
Route TOPICAL
Dosage Form KIT
RxCUI drug identifier 1043353
Application Number M017
Labeler Name Coty US LLC
Packages
Package NDC Code Description
66184-153-01 1 kit in 1 carton (66184-153-01) * 5 cloth in 1 packet * 189.9 g in 1 jar
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient 6% Benzocaine

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 Rub well (see enclosed instructions) Use wipes no more than 3 to 4 times daily. Discard wipe after use. Adults and children 13 years of age and older apply to the area to be treated 10 minutes before hair removal Children under 13 years of age consult a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients ALCOHOL DENAT., AQUA/WATER/EAU, PROPYLENE GLYCOL, METHYLPARABEN

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 temporary relief of pain and itching associated with minor skin irritations due to hair removal

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Sally Hansen Ouch-Relief Wax Kit Benzocaine Ouch-Relief Benzocaine ALCOHOL WATER DENATONIUM BENZOATE PROPYLENE GLYCOL METHYLPARABEN BENZOCAINE BENZOCAINE Ouch Relief Wax Kit FRUCTOSE DEXTROSE INVERT SUGAR SUCROSE WATER PHENOXYETHANOL GLYCERIN MICA ETHYLHEXYLGLYCERIN TITANIUM DIOXIDE HONEY ACETIC ACID COUMARIN TOCOPHEROL

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 – Kit Label New OUCH-RELIEF™ WAX KIT PAIN- RELIEF TECHNOLOGY FOR FACE AND BODY Pre-Treatment Helps Reduce Pain while Waxing Results Last Up to 8 Weeks!* Simply Rinses Off with Water *Individual hair re-growth results may vary Wax Net wt. 6.7 oz 189.9 g, 5 Benzocaine wipes, 20 Strips, 1 Spatula for face and body, Instructions Dermatologist & Salon Tested Principal Display Panel – Kit Label

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Drug Facts Other information As with all products containing benzocaine, localized allergic reactions may occur after prolonged or repeated use.

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 over raws surfaces, or blistered areas Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or comments? Call us at 1-800-953-5080 9:00AM - 5:00PM EST

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 last for more than 7 days or 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

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 Allergy Alert: do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine or other "caine" anesthetics. For external use only. Not intended for use by children under 13 years of age When using this product avoid contact with eyes Stop use and ask a doctor if condition worsens symptoms last for more than 7 days or clear up and occur again within a few days

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