FDA.reportPublic FDA data

Perfect Purity Medicated Body

Manufacturer
Davion, Inc.
Effective date
2022-12-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:45:36

Label at a glance#

ProductPerfect Purity Medicated Body
Active ingredientMENTHOL
Label structure7 sections

Indications and uses

temporarily relieves pain and itch associated with: Minor Cuts Sunburn Insect Bites Scrapes Minor Burns Minor Skin Irritations

Dosage and administration

adults and children 2 years and older apply freely up to 3 or 4 times daily. children under 2 years ask a doctor. For best results, dry skin thoroughly before applying.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 0.15%

Purpose

OTC - PURPOSE SECTION

External Analgesic

Uses

INDICATIONS & USAGE SECTION

temporarily relieves pain and itch associated with:

  • Minor Cuts
  • Sunburn
  • Insect Bites
  • Scrapes
  • Minor Burns
  • Minor Skin Irritations

Warning

WARNINGS SECTION

  • For external use only.
  • Avoid contact with eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms persists more than 7 days or clear up and occur again within a few days

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 2 years and older apply freely up to 3 or 4 times daily.
  • children under 2 years ask a doctor.
  • For best results, dry skin thoroughly before applying.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

talc, zinc oxide, eucalyptol, methyl salicylate, salicylic acid, thymol, zinc stearate.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 42669-208-01

Perfect Purity

medicated Body Powder

use daily to help skin feel fresh and healthy

NET WT 10OZ (283 g)

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42669-20842669-208-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
TALC7SEV7J4R1UIACT
ZINC OXIDESOI2LOH54ZIACT
EUCALYPTOLRV6J6604TKIACT
METHYL SALICYLATELAV5U5022YIACT
SALICYLIC ACIDO414PZ4LPZIACT
THYMOL3J50XA376EIACT
ZINC STEARATEH92E6QA4FVIACT
MENTHOLL7T10EIP3AACTIB

Source Document#

Source XML · Source PDF

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
01e25c1c-9a22-5a97-e063-6394a90a44aef166f269-22fc-4960-962e-3c70b55d281c2023-08-01WarningsExact identifier
spl set id: f166f269-22fc-4960-962e-3c70b55d281c

Reported adverse events (FAERS/openFDA)#

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