FDA.reportPublic FDA data

Vicks

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2026-10-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-10-09 01:01:56

Label at a glance#

ProductVicks Vapo Breathers
Active ingredientMENTHOL
Label structure16 sections

Indications and uses

temporarily relieves occasional minor irritation and pain due to sore throat sore mouth

Dosage and administration

adults and children 12 years and over: dissolve 1 drop slowly in the mouth. Repeat every 2 hours as needed or as directed by a doctor. children under 12 years: do not use.

Storage and handling

Store at no greater than 25°C (77°F) contains soy

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (per drop)

OTC - ACTIVE INGREDIENT SECTION

Menthol 20 mg

Purpose

OTC - PURPOSE SECTION

Oral anesthetic

Uses

INDICATIONS & USAGE SECTION

temporarily relieves occasional minor irritation and pain due to

  • sore throat
  • sore mouth

Warnings

WARNINGS SECTION

Sore Throat Warning-

SPL UNCLASSIFIED SECTION

Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult doctor promptly. Do not use more than 2 days or administer to children under 12 years of age.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • a severe sore throat accompanied by difficulty in breathing or that lasts more than 2 days
  • a sore throat accompanied by fever, headache, rash, swelling, nausea or vomiting

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • sore mouth symptoms do not improve in 7 days, or if irritation, pain, or redness persists or worsens.

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OVERDOSAGE SECTION

In case of overdose, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 12 years and over: dissolve 1 drop slowly in the mouth. Repeat every 2 hours as needed or as directed by a doctor.
  • children under 12 years: do not use.

Other information

STORAGE AND HANDLING SECTION

  • Store at no greater than 25°C (77°F)
  • contains soy

Inactive ingredients

INACTIVE INGREDIENT SECTION

acacia, ascorbyl palmitate, beta carotene, corn syrup, FD&C Blue No. 1, flavor, glycerin, maltodextrin, potassium sorbate, sucrose, sunflower oil, vitamin E DL-alpha, water

Questions?

OTC - QUESTIONS SECTION

1-800-707-1709

SPL UNCLASSIFIED SECTION

DIST. BY: PROCTER & GAMBLE, CINCINNATI, OH 45202

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VICKS®
Vapo
Breathers
MENTHOL · ORAL ANESTHETIC
VICKS VAPOR DROPS
Soothes Scratchy Throats
COOL MINT
FEEL THE SENSATION OF FREER BREATHING
40 MEDICATED DROPS

320320

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130323900040076GTIN-13: 0323900040076
EAN-13: 0323900040076
GTIN-12: 323900040076
UPC-A: 323900040076
GTIN storage (14 digits): 00323900040076		320.jpg
Data codeData Matrix21289007320.jpg

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
84126-32084126-320-40

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
SUCROSEC151H8M554IACT
ACACIA5C5403N26OIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
GLYCERINPDC6A3C0OXIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
CORN SYRUP9G5L16BK6NIACT
WATER059QF0KO0RIACT
MALTODEXTRIN7CVR7L4A2DIACT
ASCORBYL PALMITATEQN83US2B0NIACT
BETA CAROTENE01YAE03M7JIACT
SUNFLOWER OIL3W1JG795YIIACT
.ALPHA.-TOCOPHEROL, DL-7QWA1RIO01IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-05-30full-release2026-06-01 01:01:59

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
365b3ca7-a6ed-d7c9-e063-6294a90af52e365b3831-5d58-c607-e063-6294a90a39c92025-05-30WarningsExact identifier
spl set id: 365b3831-5d58-c607-e063-6294a90a39c9

Reported adverse events (FAERS/openFDA)#

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