PHARMACYS PRESCRIPTION VAPOR RUB- menthol gel

Pharmacys Prescription Vapor Rub by

Drug Labeling and Warnings

Pharmacys Prescription Vapor Rub by is a Otc medication manufactured, distributed, or labeled by American Consumer Products Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Active Ingredients

Camphor 4.7%

Menthol 1.25%

Eucalyptus Oil 1.2%

Purpose

Purpose

Decongestant

Decongestant

Decongestant

Indications & Usage

USE:

To temporarily relieve nasal congestion, chest congestion and cough due to the common cold. Temporarily relieves minor aches and pains.

Warning

Warning: For external use only. Not for internal use. Avoid contact with eyes. Do not put in mouth, nostrils, or on wounds or damaged skin.

If Pregnant or Breast Feeding

If pregnant or breast feeding, consult a physician before use. Do not use near open flame, in a microwave oven or in a container in which water is being heated except when adding to cold water in a hot steam vaporizer.

Consult a Physician Before Use

Consult a physician before use. If you have asthma, emphysema, persistent or chronic cough associated with smoking or excessive mucus. If muscle aches persist for more than 7 days or comes back, or cough lasts more than 7 days, comes back or occurs with fever, rash or a persistent headache.

Keep out of reach of children

Keep out of reach of children. If ingested, get medical help or contact a Poison Control Center right away.

Dosage & Administration

Directions:Adults and children 2 years of age and older, rub a thick layer on chest and throat for temporary relief from nasal congestion and coughing due to colds, or rub on sore aching aching muscles. If desired, loosely cover with a soft dry cloth, but keep clothing loose. Repeat up to three times daily, especially at bedtime. Children under 2 years of age, consult your physician.

Inactive Ingredients

Inactive Ingredients: Petrolatum, Thymol, Turpentine, Cedar Wood Oil, Nutmeg Oil.

Pharmacy's Prescription 4 OZ Vapor Rub

INGREDIENTS AND APPEARANCE

PHARMACYS PRESCRIPTION VAPOR RUB 
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72197-042
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	1.25 g  in 100 g
EUCALYPTUS OIL (UNII: 2R04ONI662) (EUCALYPTUS OIL - UNII:2R04ONI662)	EUCALYPTUS OIL	1.2 g  in 100 g
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	4.7 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)
NUTMEG OIL (UNII: Z1CLM48948)
CEDAR LEAF OIL (UNII: BJ169U4NLG)
TURPENTINE OIL (UNII: C5H0QJ6V7F)
THYMOL (UNII: 3J50XA376E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72197-042-04	110 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/09/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	02/09/2021

Labeler - American Consumer Products Corp (081101181)