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Clear Anti-Itch by Target Cop

Dosage form: lotion
Ingredients: PRAMOXINE HYDROCHLORIDE 1.0mL in 100L, ZINC ACETATE 0.1mL in 100L
Labeler: Target Cop
NDC Code: 11673-218

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

Uses
•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 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 no more than 3 to 4 times daily
children under 2 years - ask a doctor

Other information  store at room temperature (59⁰ - 77⁰ F)

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

 Questions?  Call 1-800-910-6874

Dist. By: target Corp., Mpls., MN 55403
Made in the USA with US + foreign components
shop Target.com

NDC 11673-213-30
anti-itch lotion
clear
Compare to active ingredients in Caladryl
external analgesic/skin protectant
drying action plus itch relief
helps relieve itching and pain
up + up
6 FL OZ (177 mL)
This product is not manufactured or distributed by Pfizer Consumer HealthCare, distributor of Caladryl Clear Lotion
CLEAR ANTI-ITCH 
pramoxine hcl, zinc acetate lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-218
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PRAMOXINE HYDROCHLORIDE (PRAMOXINE) PRAMOXINE HYDROCHLORIDE1.0 mL  in 100 L
ZINC ACETATE (ZINC CATION) ZINC ACETATE0.1 mL  in 100 L
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:11673-218-30.177 L in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34703/31/1996
Labeler - Target Cop (006961700)
Registrant - Vi-Jon (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon790752542manufacture

Revised: 05/2012
Document Id: 00e936d5-1880-4338-a28a-8e60230e8146
Set id: 2ffbe605-ad2e-418e-a78f-66c02ad8c92b
Version: 1
Effective Time: 20120501
 
Target Cop

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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 drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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