CVS Health Maximum Strength Feminine

Manufacturer
CVS Pharmacy
Effective date
2017-01-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:48:39

Label at a glance#

ProductCVS Health Maximum Strength Feminine
Active ingredientPRAMOXINE HYDROCHLORIDE
Label structure9 sections

Storage and handling

Other information store at room temperature discard within 2 months of opening

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                                              Purpose

Pramoxine hydrochloride 1% w/w......................................Extnernal analgesic

OTC - PURPOSE SECTION

Use

temporarily relieves itching

WARNINGS SECTION

Warnings

For external use only

Avoid contact with eyes

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INDICATIONS & USAGE SECTION

Directions

Adults and children 12 years of age and older: Unfold towellete and gently pat or wipes external vaginal area from front to back. Use each towelette only once and then throw away. Apply to affected area not more than 3 to 4 times daily.

Children under 12 years of age: Consult a doctor.

STORAGE AND HANDLING SECTION

Other information

  • store at room temperature
  • discard within 2 months of opening

INACTIVE INGREDIENT SECTION

Inactive ingredients

water, glycerin, phenoxyethanol, polyaminopropyl biguanide, polysorbate 20, sodium methylparaben, fragrance, benzoic acid, disodium cocamphodiacetate, dehydroacetic acid, aloe barbadensis leaf juice powder, toceopheryl acetate

DOSAGE & ADMINISTRATION SECTION

Distributed by:

CVS Pharmacy, Inc.

Once CVS Drive,

Woonsocket, RI 02895

CVS.com 1-800-SHOP CVS

Made in China

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039541pramoxine HCl 1 % Medicated PadPSN1
1039541pramoxine hydrochloride 10 MG/ML Medicated PadSCD1
1039541pramoxine hydrochloride 1 % Medicated PadSY1
1039541pramoxine hydrochloride 1 % Medicated WipeSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
58f3f9b7-3b9b-a9c1-1c9f-18ac777192b8Product name120140508
a7051cba-790b-a699-81f8-dbbbdbd9b5acProduct name120140508
da108d9e-edc8-17a3-8c28-3251c6a8acccProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69842-128-202022-01-28C16284748780-1d6a99b39-cfeb-a426-e053-dadaa90af4c264377f0a-b9af-4b6e-96f6-51c94deeb809

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-128-20CVS Health Maximum Strength Feminine20 in 1 POUCHCLOTH201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-128CVS HEALTH MAXIMUM STRENGTH FEMININE (PRAMOXINE HYDROCHLORIDE) CLOTH [CVS PHARMACY]1Legacy NDC, 1 package rows20170130_64377f0a-b9af-4b6e-96f6-51c94deeb809.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69842-12869842-128-20

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
34beab35-65b7-4419-851d-792daeee580164377f0a-b9af-4b6e-96f6-51c94deeb8092017-01-27WarningsExact identifier
spl id: 34beab35-65b7-4419-851d-792daeee5801
spl set id: 64377f0a-b9af-4b6e-96f6-51c94deeb809

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.