NOVITA 50% ISOPROPYL RUBBING ALCOHOL W/ WINTERGREEN

Manufacturer
Shield Line LLC
Effective date
2026-03-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:50:24

Label at a glance#

ProductNOVITA 50% ISOPROPYL RUBBING ALCOHOL W/ WINTERGREEN
Active ingredientISOPROPYL ALCOHOL
Label structure12 sections

Indications and uses

first aid to help prevent the risk of infection in minor cuts scrapes burns

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol (50% v/v)

OTC - PURPOSE SECTION

First Aid Antiseptic

Uses

INDICATIONS & USAGE SECTION

first aid to help prevent the risk of infection in

  • minor cuts
  • scrapes
  • burns

Warnings For external use only

WARNINGS SECTION

  • Flammable, keep away from fire and flame
  • if taken internally, serious gastric disturbances will result

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep or puncture wounds, animal bites or serious burns

When using this product

OTC - WHEN USING SECTION

  • do not get into eyes
  • do not apply over large areas of the body
  • do not use longer than one week unless directed by a doctor
  • do not use otherwise than directed

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition persists or gets worse

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed , get medical help or contact a Poison Control Center immediately

DOSAGE & ADMINISTRATION SECTION

  • clean the affected area
  • apply a small amount of this product on area 1 to 3 times daily
  • if bandaged, let dry first
  • may be covered with sterile bandage

other information

OTHER SAFETY INFORMATION

  • store at room temperature
  • does not contain, nor is intended as a substitute for grain or ethyl alcohol

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Methyl Salicylate, Laneth-75, FD&C Yellow#5

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display PanelPrincipal Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616456isopropyl alcohol 50 % Topical SolutionPSN4
616456isopropyl alcohol 0.5 ML/ML Topical SolutionSCD4
616456isopropyl alcohol 50 % Topical SolutionSY4

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130352410105142GTIN-13: 0352410105142
EAN-13: 0352410105142
GTIN-12: 352410105142
UPC-A: 352410105142
GTIN storage (14 digits): 00352410105142
32-10514NVP-01.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52410-1051-4NOVITA 50% ISOPROPYL RUBBING ALCOHOL W/ WINTERGREEN355 mL in 1 BOTTLELIQUID3554
52410-1051-6NOVITA 50% ISOPROPYL RUBBING ALCOHOL W/ WINTERGREEN475 mL in 1 BOTTLELIQUID4754

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
52410-105152410-1051-4, 52410-1051-6

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

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
NOVITA 50% ISOPROPYL RUBBING ALCOHOL W/ WINTERGREENISOPROPYL ALCOHOLShield Line LLC3bd9fc61-b135-51f5-e054-00144ff8d46c2026-03-17WarningsExact identifier
ndc (package): 52410-1051-6
ndc (package): 52410-1051-4
ndc (product): 52410-1051
ndc11 (package): 52410105104
ndc11 (package): 52410105106
spl id: 4d3c0c2e-14a2-636d-e063-6394a90a0935
spl set id: 3bd9fc61-b135-51f5-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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