Vicks ®VapoRub™ ADVANCED PLUS

Vicks VapoRub ADVANCED PLUS by

Drug Labeling and Warnings

Vicks VapoRub ADVANCED PLUS by is a Otc medication manufactured, distributed, or labeled by Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

VICKS VAPORUB ADVANCED PLUS- camphor, eucalyptus oil, menthol ointment 
Procter & Gamble Manufacturing Company

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Vicks ®VapoRub™ ADVANCED PLUS

Drug Facts

Active ingredients

Camphor (synthetic) 4.8%
Eucalyptus oil 1.2%
Menthol 2.6%

Active ingredients Purpose

Cough suppressant & topical analgesic
Cough suppressant
Cough suppressant & topical analgesic

Uses

when applied to chest and throat, temporarily relieves cough due to minor throat and bronchial irritation associated with the common cold
when applied to muscles and joints, temporarily relieves minor aches and pains of muscles and joints

Warnings

For external use only; avoid contact with eyes.

Do not use

by mouth

in nostrils

on wounds or damaged skin

with tight bandages

Ask a doctor before use if you have

cough that occurs with too much phlegm (mucus)

persistent or chronic cough such as occurs with smoking, asthma or emphysema

When using this product

do not

heat

microwave

add to hot water or any container where heating water. May cause splattering and result in burns.

Stop use and ask a doctor if

muscle aches and pains worsen or persist for more than 7 days or clear up and occur again within a few days.

cough persists for more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent headache. A persistent cough may be a sign of a serious condition.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

see important warnings under “When using this product”

adults and children 2 years and over:

for cough suppression rub a thick layer on throat & chest

cover with a warm, dry cloth if desired

keep clothing loose about throat and chest to help vapors reach the nose and mouth

use up to three times daily or as directed by doctor

for muscle / joint minor aches and pains apply to affected area not more than 3 to 4 times daily

children under 2 years: do not use

Other information

store at no greater than 25°C (77°F)

Inactive ingredients

cedarleaf oil, nutmeg oil, paraffin, petrolatum, Symcool ®WS-5 (menthane carboxamidoethyl acetate), thymol, turpentine oil

Questions?

1-800-873-8276

TAMPER EVIDENT: CARTON SEALED FOR YOUR PROTECTION

MADE IN GERMANY
DIST. BY: PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 2.82 OZ (80 g) jar

NEW

VICKS ®

VapoRub™

ADVANCED PLUS

COUGH SUPPRESSANT

TOPICAL ANALGESIC

POWERFUL COUGH RELIEF

VAPORS LAST UP TO 8 HOURS

NET WT 2.82 OZ (80 g)

OINTMENT

VICKS VAPORUB ADVANCED PLUS 
camphor, eucalyptus oil, menthol ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-793
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EUCALYPTUS OIL (UNII: 2R04ONI662) (EUCALYPTUS OIL - UNII:2R04ONI662)	EUCALYPTUS OIL	0.012 g  in 1 g
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	0.026 g  in 1 g
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	0.048 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
N-((ETHOXYCARBONYL)METHYL)-P-MENTHANE-3-CARBOXAMIDE (UNII: Q6CA504696)
PARAFFIN (UNII: I9O0E3H2ZE)
TURPENTINE OIL (UNII: C5H0QJ6V7F)
PETROLATUM (UNII: 4T6H12BN9U)
THYMOL (UNII: 3J50XA376E)
CEDAR LEAF OIL (UNII: BJ169U4NLG)
NUTMEG OIL (UNII: Z1CLM48948)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-793-01	1 in 1 CARTON	07/06/2023	07/06/2023
1		50 g in 1 JAR; Type 0: Not a Combination Product
2	NDC: 69423-793-02	1 in 1 CARTON	07/06/2023	07/06/2023
2		80 g in 1 JAR; Type 0: Not a Combination Product
3	NDC: 69423-793-03	2 in 1 CELLO PACK	07/06/2023	07/06/2023
3		80 g in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	07/06/2023	07/06/2023

Labeler - Procter & Gamble Manufacturing Company (004238200)

Revised: 12/2023

Document Id: 0b7644d3-9fd6-b562-e063-6294a90ae44b

34390-5

Set id: 0036d6fc-eed6-ee87-e063-6294a90a8022

Version: 6

Effective Time: 20231201

 

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