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CVS Fragrance Free Anti-Itch by RITE AID CORPORATION

Medically reviewed on July 9, 2018

Dosage form: lotion
Ingredients: PRAMOXINE HYDROCHLORIDE 10mg in 1mL
Labeler: RITE AID CORPORATION
NDC Code: 11822-0405

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                                 Purpose

Pramoxine Hydrochloride 1%............................External Analgesic




Uses


For the temporary relief of itching associated with minor skin irritations


Keep out of reach of children. If swallowed, get medical help or contact a
Poison Control Center right away.



Uses

For the temporary relief of itching associated with minor skin irritations

Warnings

For external use only

When using this product

- avoid contact with eyes

Stop use and ask a doctor if
- condition worsens
- symptoms persist for 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

adults and children 2 years and older

- apply to affected area not more than 3 to 4 times daily

children under 2 years of age

- consult a doctor


Inactive Ingredients

benzyl alcohol, carbomer, cetyl alcohol, dimethicone, glycerul stearate, isopropyl myristate,
PEG-8, PEG-100 stearate, petrolatum, purified water, sodium hydroxide, stearic acid



CVS FRAGRANCE FREE ANTI-ITCH 
pramoxine hydrochloride lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-0405
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PRAMOXINE HYDROCHLORIDE (PRAMOXINE) PRAMOXINE HYDROCHLORIDE10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
CARBOMER HOMOPOLYMER TYPE C 
ISOPROPYL MYRISTATE 
GLYCERYL MONOSTEARATE 
STEARIC ACID 
CETYL ALCOHOL 
PETROLATUM 
DIMETHICONE 350 
POLYETHYLENE GLYCOL 400 
BENZYL ALCOHOL 
SODIUM HYDROXIDE 
POLYETHYLENE GLYCOL 4500 
Packaging
#Item CodePackage Description
1NDC:11822-0405-9222 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34807/08/2010
Labeler - RITE AID CORPORATION (014578892)
Registrant - Pharma Pac, LLC (140807475)
Establishment
NameAddressID/FEIOperations
Pharma Pac, LLC140807475manufacture

 
RITE AID CORPORATION

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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