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Clear Anti-Itch by Liberty Procurement, Inc

Medically reviewed on September 22, 2016

Dosage form: lotion
Ingredients: PRAMOXINE HYDROCHLORIDE 1mg in 1mL, ZINC ACETATE 0.1mg in 1mL
Labeler: Liberty Procurement, Inc
NDC Code: 63940-952

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Active ingredients

Pramoxine HCl 1%

Zinc acetate 0.1%

Purpose

External analgesic

Skin protectant

Purpose
  • for the temporary relief of pain and itching associated with minor skin irritations and rashes due to poison ivy, poison oak or poison sumac
  • dries the oozing and weeping of poison: - ivy - oak - sumac

Warnings

For external use only

When using this product
  • do not get into eyes

Stop use section and ask a doctor if
  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children

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

Directions
  • shake well
  • before applying wash affected area of skin

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 - ask a doctor

Other information

store at room temperature (59° - 77° F)

inactive ingredients

alcohol, camphor, citric acid, diazolidinyl urea, fragrance, glycerin, hydroxypropyl methylcellulose, methylparaben, oil of lavender, oil of rosemary, polysorbate 40, propylene glycol, propylparaben purified water, sodium citrate

Adverse reactions

Distributed by

Liberty Procurement, Inc

650 Liberty Ave.

Union, NJ 07083 USA

Visit us at:

www.facevalues.com

SATISFACTION

GUARANTEED

Or Your

Money Back

Principal Display Panel

CORE VALUES

CLEAR

Itch Relief

Lotion

EXTERNAL ANALGESIC

SKIN PROTECTANT

Drying action

PLUS itch relief

6 FL OZ (177 mL)

CLEAR ANTI-ITCH 
pramoxine hcl, zinc acetate lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63940-952
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PRAMOXINE HYDROCHLORIDE (PRAMOXINE) PRAMOXINE HYDROCHLORIDE1 mg  in 1 mL
ZINC ACETATE (ZINC CATION) ZINC ACETATE0.1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL 
CAMPHOR (SYNTHETIC) 
CITRIC ACID MONOHYDRATE 
DIAZOLIDINYL UREA 
GLYCERIN 
HYPROMELLOSES 
METHYLPARABEN 
LAVENDER OIL 
ROSEMARY OIL 
POLYSORBATE 40 
PROPYLENE GLYCOL 
PROPYLPARABEN 
WATER 
SODIUM CITRATE 
Packaging
#Item CodePackage Description
1NDC:63940-952-30177 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34703/17/2011
Labeler - Liberty Procurement, Inc (804085293)
Registrant - Vi-Jon (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon790752542manufacture(63940-952)

 
Liberty Procurement, Inc

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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