Puricia

Manufacturer
PHARMABERG INC.
Effective date
2020-11-27
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:53:28

Label at a glance#

ProductPuricia
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

To decrease bacteria on the skin that could cause disease. Recommended for repeated use.

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping. for children under 6, use only under adult supervision not recommended for infants.

Storage and handling

do not store above 105°F may discolor some fabrics. harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • To decrease bacteria on the skin that could cause disease.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only: hands

Flammable. Keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product

  • keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • avoid contact with broken skin.
  • do not inhale or ingest.

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • irritation or redness develop.
  • condition persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands thoroughly with product and allow to dry without wiping.
  • for children under 6, use only under adult supervision
  • not recommended for infants.

Other information

STORAGE AND HANDLING SECTION

  • do not store above 105°F
  • may discolor some fabrics.
  • harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol, Carbomer.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60 ml NDC: 77302-001-01 60 ml front label60 ml front label60 ml NDC: 77302-001-01 60 ml Back label60 ml Back label

100 ml NDC: 77302-001-02 100 ml Front label100 ml Front label100 ml NDC: 77302-001-02 100 ml Back label100 ml Back label

237 ml NDC: 77302-001-03 237 ml front label237 ml front label

237 ml NDC: 77302-001-03 237 ml back label237 ml back label

500 ml NDC: 77302-001-04 500 ml front label500 ml front label500 ml NDC: 77302-001-04 500 ml back label500 ml back label1000 ml NDC: 77302-001-05 1000 ml front label1000 ml front label1000 ml NDC: 77302-001-05 1000 ml back label1000 ml back label

3.78 L NDC: 77302-001-06 3.78 L front label3.78 L front label3.78 L NDC: 77302-001-06 3.78 L back label3.78 L back label

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77302-00177302-001-01, 77302-001-02, 77302-001-03, 77302-001-04, 77302-001-05, 77302-001-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
c4e7a662-2ea2-5e00-e053-2a95a90afb7da4a63089-d110-1554-e053-2995a90a0aad2021-06-16WarningsExact identifier
spl set id: a4a63089-d110-1554-e053-2995a90a0aad

Reported adverse events (FAERS/openFDA)#

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