Sally Hansen Ouch-Relief description, usages, side effects, indications, overdosage, supplying and lots more!

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Sally Hansen Ouch-Relief

Coty US LLC


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

6% Benzocaine

Purpose

Topical Analgesic

Uses

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

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

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.

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

Other information

As with all products containing benzocaine, localized allergic reactions may occur after prolonged or repeated use.

Inactive ingredients

ALCOHOL DENAT., AQUA/WATER/EAU, PROPYLENE GLYCOL, METHYLPARABEN

Questions or comments?

Call us at 1-800-953-5080 9:00AM - 5:00PM EST

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

Sally Hansen Ouch-Relief

Benzocaine KIT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:66184-153
Route of Administration TOPICAL DEA Schedule

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:66184-153-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partB part333B 2012-01-01


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Be sure to consult your doctor before taking any medication!
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