FDA.reportPublic FDA data

Vicks ® Herbal Drops

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 01:01:52

Label at a glance#

ProductVicks Herbal Drops
Active ingredientMENTHOL
Label structure16 sections

Indications and uses

temporarily relieves cough associated with a cold occassional minor irritation and pain due to sore throat or sore mouth

Dosage and administration

adults and children 12 years and over: dissolve 2 drops (one at a time) slowly in the mouth. Repeat every 2 hours as needed or as directed by a doctor. children 12 years and under: do not use

Storage and handling

Store at no greater than 25°C (77°F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (per drop)

OTC - ACTIVE INGREDIENT SECTION

Menthol 4.8 mg

Purpose

OTC - PURPOSE SECTION

Cough Suppresesant/Oral anesthetic

Uses

INDICATIONS & USAGE SECTION

temporarily relieves

  • cough associated with a cold
  • occassional minor irritation and pain due to sore throat or 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

  • persistent or chronic cough such as occurs with smoking, asthma, or emphysema
  • cough accompanied by excessive phlegm (mucus)
  • 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

  • cough persists more than 1 week, tends to rcur, or is accompaned by fever, rash, or persistent headache
  • 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 2 drops (one at a time) slowly in the mouth. Repeat every 2 hours as needed or as directed by a doctor.
  • children 12 years and under: do not use

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

caramel, corn syrup, flavors (with extracts of Elderflower, Horehound, Hyssop, Lemon balm, Linden Flower, Marshmallow Root, Peppermint, Sage and Thyme), propylene glycol, sucrose, 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 ®

Herbal Drops

MENTHOL • COUGH SUPPRESSANT/ORAL ANESTHETIC

COUGH RELIEF

ALPINE SPRING

HERBAL BLEND

PEPPERMINT • ELDERFLOWER • LEMON BALM

Sage, Linden Flower, Horehound, Hyssop, Thyme, Marshmallow Root

50 DROPS

323323

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130323900039919GTIN-13: 0323900039919
EAN-13: 0323900039919
GTIN-12: 323900039919
UPC-A: 323900039919
GTIN storage (14 digits): 00323900039919		323.jpg
Data codeData Matrix21309608323.jpg

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
84126-32384126-323-50

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
SUCROSEC151H8M554IACT
CORN SYRUP9G5L16BK6NIACT
CARAMELT9D99G2B1RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-07-01full-release2026-06-01 01:07:12

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
38dd4fa9-8b75-47b6-e063-6294a90a1b7b38dd9678-75e8-ac3b-e063-6394a90a72a62025-07-01WarningsExact identifier
spl set id: 38dd9678-75e8-ac3b-e063-6394a90a72a6

Reported adverse events (FAERS/openFDA)#

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