Quit Nits Preventative description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Quit Nits Preventative

Wild Child W A Pty Ltd
Wild Child W A Pty Ltd

DRUG FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS

Eucalyptus globulus 1X (Tasmanian Blue Gum 1mg/g)

PURPOSE

Lice prevention

USE


WARNINGS

For external use only.

DO NOT USE

  • near eyes
  • inside the nose, mouth or vagina
  • on lice in eyebrows or eyelashes

See a doctor if lice are present in these areas.



WHEN USING THIS PRODUCT

  • keep tightly closed and protect eyes with a washcloth or towel.
  • if product gets into the eyes, flush with water right away.

STOP USE AND ASK A DOCTOR IF

  • eye irritation occurs
  • skin or scalp irritation continues or infection occurs



KEEP OUT OF REACH OF CHILDREN

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

DIRECTIONS

Apply


Comb


Repeat

OTHER INFORMATION

  • keep carton for important product information
  • protect from excessive heat

INACTIVE INGREDIENTS


QUESTIONS

800-961-4936 or

support@QuitNits.com

www.QuitNits.com

PACKAGING INFORMATION



















  • children
  • hats/clothes
  • bedding
  • toys

  • Contains natural essential oils
  • No chemical pesticides
  • Pleasant fragrance
  • Low allergy formulation


Leanne Preston, Founder
"
We believe that Wild Child's acknowledgment of our need to exist as part of nature, our hopes for the world and our responsibility to its children are the reasons for our being and the motivations for our growth."




Does NOT Contain:


Wild Child (US) Pty Ltd









Quit Nits Preventative


Quit Nits Preventative

eucalyptus globulus SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:30807-3003
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
EUCALYPTUS GLOBULUS LEAF EUCALYPTUS GLOBULUS LEAF 1 [HP_X]

Inactive Ingredients

Ingredient Name Strength
water
POLYSORBATE 20
ACETIC ACID
ALCOHOL
DIMETHICONE
CETRIMONIUM CHLORIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 125 in 1 BOTTLE, SPRAY
2 NDC:30807-3003-4 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2008-01-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.