Vicks® VapoFreeze™ Pain Relieving Spray

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2026-10-05
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
daily-update
Hydrated at
2026-10-07 01:02:28

Label at a glance#

ProductVicks VapoFreeze PAIN RELIEVING
Active ingredientMENTHOL, CAMPHOR (SYNTHETIC)
Label structure14 sections

Dosage and administration

adults and children over 12 years of age and older: spray the affected area not more than 3 to 4 times daily product will dry quickly on its own, and does not need to be rubbed in wash hands thoroughly with soap and water after each use children under 12 years of age: ask a doctor Store at no greater than 25°C (77°F).

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 3.6%

Menthol 16%

Active ingredients Purpose

OTC - PURPOSE SECTION

Topical anesthetic

Topical analgesic

Use

INDICATIONS & USAGE SECTION

temporarily relieves minor pain aches and pains of muscles and joints associated with:

  • arthritis 
  • simple backache
  • strains
  • sprains
  • bruises

provides penetrating pain relief

Warnings

WARNINGS SECTION

For external use only
Extremely flammable: keep away from fire, sparks, and heated surfaces. Contents under pressure, do not puncture or incinerate container. Exposure to temperatures above 120° may cause bursting.

Do not use

OTC - DO NOT USE SECTION

  • on wounds or on irritated or damaged skin
  • with a heating pad

When using this product

OTC - WHEN USING SECTION

  • use only as directed. Intentional misuse by deliberately concentrating or inhaling the contents can be harmful or fatal.
  • do not bandage tightly
  • avoid contact with eyes and mucous membranes. Do not spray in face or mouth.
  • do not expose the area to local heat or direct sunlight
  • rare cases of serious burns have been reported with products of this type
  • a transient burning sensation may occur upon application but generally disappears in several days
  • avoid applying into skin folds

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens or symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days
  • redness is present or excessive skin irritation occurs
  • you experience severe burning pain, swelling, or blistering where the product was applied

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.

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children over 12 years of age and older:

  • spray the affected area not more than 3 to 4 times daily
  • product will dry quickly on its own, and does not need to be rubbed in
  • wash hands thoroughly with soap and water after each use

children under 12 years of age:ask a doctor

Store at no greater than 25°C (77°F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol denat., fragrance, isopropyl myristate, propylene glycol, water

Questions?

OTC - QUESTIONS SECTION

1-855-446-4345

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 3 OZ

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VICKS ®

Vapo

Freeze™

PAIN RELIEVING SPRAY

MAX STRENGTH MENTHOL‡ + CAMPHOR

PAIN RELIEF SPRAY

QUICK-DRYING

NET WT 3 OZ (85 g)

303303

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130030772144619GTIN-13: 0030772144619
EAN-13: 0030772144619
GTIN-12: 030772144619
UPC-A: 030772144619
GTIN storage (14 digits): 00030772144619
303.jpg
QR code linkQR Codescan.pg.com/01/00030772144619303.jpg
Data codeData Matrix21481522303.jpg

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
84126-30384126-303-03

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42026-03-19full-release2026-06-01 01:50:44

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
4d6279b8-e671-0020-e063-6394a90aaf284038e50d-b53b-4f56-b54e-62157e286e082026-03-19WarningsExact identifier
spl set id: 4038e50d-b53b-4f56-b54e-62157e286e08

Reported adverse events (FAERS/openFDA)#

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