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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vapourising 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

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

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

Directions

Inactive ingredients

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

PRINCIPAL DISPLAY PANEL

VAPORISING CHEST RUB
NASAL DECONGESTANT AND COUGH SUPPRESSANT
NET WT.4 OZ (113g)

PRINCIPAL DISPLAY PANEL



VAPORIZING CHEST RUB 
menthol and camphor and eucalyptus oil gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-012
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 g  in 100 g
EUCALYPTUS OIL (UNII: 2R04ONI662) (EUCALYPTUS OIL - UNII:2R04ONI662) EUCALYPTUS OIL1 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:52000-012-0850 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/15/2022
2NDC:52000-012-0956.6 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/15/2022
3NDC:52000-012-10100 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/15/2022
4NDC:52000-012-11113 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/15/2022
5NDC:52000-012-12150 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/15/2022
6NDC:52000-012-13170 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/15/2022
7NDC:52000-012-14226 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/15/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34103/15/2013
Labeler - Universal Distribution Center LLC (019180459)
Registrant - Anicare Pharmaceuticals Pvt. Ltd (916837425)
Establishment
NameAddressID/FEIBusiness Operations
Jell Pharmaceuticals Pvt. Ltd.726025211manufacture(52000-012)
Establishment
NameAddressID/FEIBusiness Operations
Anicare Pharmaceuticals Pvt. Ltd916837425manufacture(52000-012)

Revised: 11/2022
Document Id: ee0c344b-bac1-0f81-e053-2a95a90a9c7b
Set id: d1b1c91e-d101-48bd-b4e0-ed8b3706f990
Version: 5
Effective Time: 20221122
 
Universal Distribution Center LLC