SELVAN85

Manufacturer
Terra Hydrochem Inc.
Effective date
2022-10-26
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:50:28

Label at a glance#

ProductSELVAN85
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Pump a small amount of product into palm of hand Rub thoroughly over all surfaces of both hands Rub hands together briskly until dry

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops, or if conditions persist 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 Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Pump a small amount of product into palm of hand
  • Rub thoroughly over all surfaces of both hands
  • Rub hands together briskly until dry

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera plus proprietary blend

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin

Recommended for repeated use

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59 mL NDC: 90095-001-02

59 mL59 mL59 mL BACK59 mL BACK

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3.63 L NDC: 9005-003-01

3.63L FRONT3.63L FRONT3.63 L BACK3.63 L BACK

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

236 mL NDC: 90095-002-08

236 mL FRONT Label236 mL FRONT Label236 mL_BACK236 mL_BACK

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90095-00190095-001-02, 90095-001-08, 90095-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
f8988458-05bf-be69-e053-6394a90ab032ac0fd1e3-afc8-f0e4-e053-2a95a90acabd2023-04-05WarningsExact identifier
spl set id: ac0fd1e3-afc8-f0e4-e053-2a95a90acabd

Reported adverse events (FAERS/openFDA)#

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