ALLURE VAPORIZING CHEST RUB- menthol and camphor and eucalyptus oil gel

Allure Vaporizing Chest Rub by

Drug Labeling and Warnings

Allure Vaporizing Chest Rub by is a Otc medication manufactured, distributed, or labeled by Universal Distribution Center LLC, Anicare Pharmaceuticals Pvt. Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Camphor            4.7%

Menthol             1.0%

Eucalyptus Oil   1.0%

Purpose

Decongestant

Uses

• on chest and throat, helps temporarily relive cough due to common cold.
  
• on joints and muscles, temporarily relives minor aches and pains.

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,

• cough that occurs with too much phlegm (mucus)
• persistent or chronic cough such as occurs with asthma, emphysema, or smoking

When using this product,do not

• heat
• microwave
• add to hot water or any container where heating water. May cause splattering and results in burns
  

Stop use and ask a doctor if

• cough lasts more than 7 days, comes back, or occurs with fever, rash or persistent headache. These could be signs of a serious conditions
• muscle aches or pain persist more than 7 days or come back
  

Keep out of the reach of children

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

Directions

• adults and children 2 years and over
• rub a thick layer on chest and throat or rub on sore aching muscles
  
• repeat up to 3 times per 24 hours or as directed by doctor
  
• do not use on children under 2 years unless directed by doctor

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)

INGREDIENTS AND APPEARANCE

ALLURE VAPORIZING CHEST RUB 
menthol and camphor and eucalyptus oil gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52000-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	4.7 g  in 100 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1.0 g  in 100 g
EUCALYPTUS OIL (UNII: 2R04ONI662) (EUCALYPTUS OIL - UNII:2R04ONI662)	EUCALYPTUS OIL	1.0 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-003-08	50 g in 1 BOTTLE, PLASTIC
2	NDC: 52000-003-09	56.6 g in 1 BOTTLE, PLASTIC
3	NDC: 52000-003-10	100 g in 1 BOTTLE, PLASTIC
4	NDC: 52000-003-11	113 g in 1 BOTTLE, PLASTIC
5	NDC: 52000-003-12	150 g in 1 BOTTLE, PLASTIC
6	NDC: 52000-003-13	170 g in 1 BOTTLE, PLASTIC
7	NDC: 52000-003-14	226 g in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	06/30/2012

Labeler -  Universal Distribution Center LLC (019180459)

Establishment
Name	Address	ID/FEI	Business Operations
Anicare Pharmaceuticals Pvt. Ltd		916837425	manufacture(52000-003)