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Itch Relief Medicated Pads CVS

Dosage form: liquid
Ingredients: PRAMOXINE HYDROCHLORIDE 1g in 100g, ZINC ACETATE .1g in 100g
Labeler: CVS
NDC Code: 69842-842

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 ingredient

Pramoxine  HCl 1%               External Analgesic

Zinc Acetate 0.1%                 Skin Pretectant

Uses
  • Temporarily relieves pain and itching asociated with:
  • rashes due to poison ivy, poison oak or poison sumac.
  • insect bites.
  • minor skin irritation.
  • minor cuts.
  • dries the oozing and weeping of poison ivy, poison oak and poison sumac.

Warnings

For external use only.

Flammable: Do not use near heat, flame, or while smoking.

​​​

When using this product
  • keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if
  • condition worsens or does not improve within 7 days.
  • symptoms persist for more than 7 days or clear up and occur again with in a few days.

Keep out of reach of children

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

Directions

  • 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 of age: ask a doctor. 

Inactive ingredients

Avena Sativa (Oat) Meal Extract
Camphor
Citric Acid
Diazolidinyl Urea
Fragrance
Glycerin
Hydroxypropyl Methylcellulose
Methylparaben
Polysorbate 40
Propylene Glycol
Propylparaben
SD Alcohol 38-B
Sodium Citrate
Water

ITCH RELIEF MEDICATED PADS  CVS
pramoxine hcl, zinc acetate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-842
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PRAMOXINE HYDROCHLORIDE (PRAMOXINE) PRAMOXINE HYDROCHLORIDE1 g  in 100 g
ZINC ACETATE (ZINC CATION) ZINC ACETATE.1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL 
OATMEAL 
CAMPHOR (SYNTHETIC) 
CITRIC ACID MONOHYDRATE 
DIAZOLIDINYL UREA 
GLYCERIN 
HYPROMELLOSE, UNSPECIFIED 
METHYLPARABEN 
POLYSORBATE 40 
PROPYLENE GLYCOL 
PROPYLPARABEN 
SODIUM CITRATE 
WATER 
Packaging
#Item CodePackage Description
1NDC:69842-842-0369 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34703/15/2017
Labeler - CVS (062312574)
Registrant - Product Quest Mfg, LLC (927768135)
Establishment
NameAddressID/FEIOperations
Product Quest Mfg, LLC927768135manufacture(69842-842)

Revised: 11/2017
 
CVS

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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