Softlips description, usages, side effects, indications, overdosage, supplying and lots more!

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Softlips

The Mentholatum Company
The Mentholatum Company

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients

Octinoxate 7.5%

Octisalate 5%

Purpose

Octinoxate - Sunscreen

Octisalate - Sunscreen

Softlips Uses

  • •helps prevent sunburn

Warnings

Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging.This product has been shown only to prevent sunburn, not skin cancer or early skin aging.

For external use only

Do not use

on damaged or broken skin

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

rash occurs

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • •apply liberally 15 minutes before sun exposure
  • •use a water resistant sunscreen if swimming or sweating
  • •reapply at least every 2 hours
  • •children under 6 months: ask a doctor

Softlips Other information

  • •protect this product from excessive heat and direct sun

Inactive ingredients

lanolin oil, hydrogenated polyisobutene, ozokerite, limnanthes alba (meadowfoam) seed oil, VP/hexadecene copolymer, mineral oil, bis-diglyceryl polyacyladipate-2, oleyl alcohol, copernicia cerifera (carnauba) wax, ricinus communis (castor) seed oil, cetyl lactate, polyethylene, paraffin, ammonium glycyrrhizate, BHT, butylparaben, flavor, isobutylparaben, isopropylparaben, menthol, tocopheryl acetate [vitamin E], bismuth oxychloride,carmine, mica, titanium dioxide

Questions?

Toll free 1-877-636-2677 MON-FRI 9AM-5PM (EST) softlips.com

Principal Display Panel

Principal Display Panel

Softlips

octinoxate, octisalate STICK

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10742-8563
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 75 mg
OCTISALATE OCTISALATE 50 mg

Inactive Ingredients

Ingredient Name Strength
LANOLIN OIL
HYDROGENATED POLYBUTENE (1300 MW)
Ceresin
OLEYL ALCOHOL
HEXADECYL POVIDONE (4 HEXADECYL BRANCHES/REPEAT)
MEADOWFOAM SEED OIL
Mineral Oil
carnauba wax
castor oil
Cetyl Lactate
PARAFFIN
AMMONIUM GLYCYRRHIZATE
BUTYLATED HYDROXYTOLUENE
BISMUTH OXYCHLORIDE
BUTYLPARABEN
isobutylparaben
ISOPROPYLPARABEN
MENTHOL
.ALPHA.-TOCOPHEROL
MICA
titanium dioxide

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 2 in 1 TUBE
2 2 in 1 TUBE
3 NDC:10742-8563-2 2 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2010-02-01


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