VAPOREX- camphor (synthetic), eucalyptus oil, and menthol ointment 
DLC Laboratories, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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VAPOREX®

Drug Facts

Active IngredientsPurposes
Camphor 4.8%Cough suppressant & topical analgesic
Eucalyptus Oil 1.2%Cough suppressant
Menthol 2.6%Cough suppressant & topical analgesic

Uses

Warnings

For external use only; avoid contact with eyes.

Do not use

  • by mouth
  • with tight bandages
  • in nostrils
  • on wounds or damaged skin

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 lasts more than 7 days, comes back, or occurs with 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 immediately.

Directions

See important warnings under "When using this product."

Children under 2 years: do not use

Other information

Inactive ingredients

cedarleaf oil, nutmeg oil, paraffin wax, petrolatum, thymol, turpentine oil

Manufactured by:
DLC Laboratories
Paramount, CA 90723 USA

PRINCIPAL DISPLAY PANEL - 56.7 g Jar Carton

FOR ADULTS & CHILDREN

MEDICATED CHEST RUB

Triple Action Relief

VAPOREX®

• OINTMENT •

NO ARTIFICIAL COLORS
OR FRAGRANCES

COUGH SUPPRESSANT
TOPICAL ANALGESIC

NET WT 2.0 OZ (56.7 g)

PRINCIPAL DISPLAY PANEL - 56.7 g Jar Carton
VAPOREX 
camphor (synthetic), eucalyptus oil, and menthol ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24286-1564
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)4.8 g  in 100 g
EUCALYPTUS OIL (UNII: 2R04ONI662) (EUCALYPTUS OIL - UNII:2R04ONI662) EUCALYPTUS OIL1.2 g  in 100 g
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM2.6 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
PARAFFIN (UNII: I9O0E3H2ZE)  
PETROLATUM (UNII: 4T6H12BN9U)  
CEDAR LEAF OIL (UNII: BJ169U4NLG)  
NUTMEG OIL (UNII: Z1CLM48948)  
THYMOL (UNII: 3J50XA376E)  
TURPENTINE OIL (UNII: C5H0QJ6V7F)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24286-1564-21 in 1 CARTON03/12/201311/07/2017
162.5 g in 1 JAR; Type 0: Not a Combination Product
2NDC:24286-1564-31 in 1 CARTON03/12/2013
256.7 g in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34103/12/2013
Labeler - DLC Laboratories, Inc. (093351930)
Establishment
NameAddressID/FEIBusiness Operations
DLC Laboratories, Inc.093351930MANUFACTURE(24286-1564) , LABEL(24286-1564)

Revised: 11/2017
Document Id: d633f94b-838f-46e0-a89e-8ab65301fe2b
Set id: 971943b1-4199-4f75-9d2d-61242d346b5f
Version: 2
Effective Time: 20171129
 
DLC Laboratories, Inc.