ALLURE VAPORIZING CHEST RUB - menthol and camphor and eucalyptus oil gel 
Universal Distribution Center LLC

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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ALLURE VAPORIZING CHEST RUB

Active Ingredients

Camphor            4.7%

Menthol             1.0%

Eucalyptus Oil   1.0%

Purpose

Decongestant

Uses


Warnings

For external use only; avoid contact with eyes.

Do not use
  • by mouth
  • in nostrils
  • with tight bandages
  • on wounds or damaged skin

Ask doctor before use if you have,

When using this product,do not

Stop use and ask a doctor if

Keep out of the reach of children

In ingested get medical help or contact a Poison control center immediately

Directions


Inactive ingredient

cedar oil, nutmeg oil, paraffin, petrolatum, thymol, turpentine oil

PRINCIPAL DISPLAY PANEL

ALLURE VAPORISING CHEST RUB
DECONGESTANT AND COUGH SUPPRESSANT
4 FL.OZ (113 GRAM)
PRINCIPAL DISPLAY PANEL



ALLURE VAPORIZING CHEST RUB 
menthol and camphor and eucalyptus oil gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)4.7 g  in 100 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1.0 g  in 100 g
EUCALYPTUS OIL (UNII: 2R04ONI662) (EUCALYPTUS OIL - UNII:2R04ONI662) EUCALYPTUS OIL1.0 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CEDAR LEAF OIL (UNII: BJ169U4NLG)  
NUTMEG OIL (UNII: Z1CLM48948)  
MINERAL OIL (UNII: T5L8T28FGP)  
PETROLATUM (UNII: 4T6H12BN9U)  
THYMOL (UNII: 3J50XA376E)  
TURPENTINE OIL (UNII: C5H0QJ6V7F)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52000-003-0850 g in 1 BOTTLE, PLASTIC
2NDC:52000-003-0956.6 g in 1 BOTTLE, PLASTIC
3NDC:52000-003-10100 g in 1 BOTTLE, PLASTIC
4NDC:52000-003-11113 g in 1 BOTTLE, PLASTIC
5NDC:52000-003-12150 g in 1 BOTTLE, PLASTIC
6NDC:52000-003-13170 g in 1 BOTTLE, PLASTIC
7NDC:52000-003-14226 g in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34106/30/2012
Labeler -  Universal Distribution Center LLC (019180459)
Establishment
NameAddressID/FEIBusiness Operations
Anicare Pharmaceuticals Pvt. Ltd916837425manufacture(52000-003)

Revised: 6/2012
Document Id: 47d12679-b500-4813-b53d-c9d4e1d1bcde
Set id: decdda4c-f46f-497f-8ddd-1ecc5d0b716c
Version: 1
Effective Time: 20120630
 
Universal Distribution Center LLC