RUBBING ALCOHOL 50 PERCENT WITH WINTERGREEN- isopropyl alcohol liquid 
Viny Health and Beauty Products 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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Active ingredient (BY VOLUME)

ISOPROPYL ALCOHOL (50% CONCENTRATE)

Purpose

TOPICAL ANTIMICROBIAL

Uses

  • TO DECREASE GERMS IN MINOR CUTS AND SCRAPES.
  • HELPS RELIEVE MUSCULAR ACHES DUE TO EXERTION.

Keep Out of Reach of Children

IN CASE OF AN ACCIDENTAL INGESTION, CONTACT A POISON CONTROL CENTER IMMEDIATELY.

WARNINGS

For external use only.

  • FLAMMABLE, KEEP AWAY FROM FIRE AND FLAME
  • IF TAKEN INTERNALLY SERIOUS GASTRIC DISTURBANCES WILL RESULT

ASK A DOCTOR BEFORE USE IF YOU HAVE

  • DEEP PUNCTURE WOUNDS SERIOUS BURNS

WHEN USING THIS PRODUCT

  • DO NOT GET INTO EYES OR MUCOUS MEMBRANES
  • USE ONLY IN A WELL-VENTILLATED AREA.

STOP USE AND ASK A DOCTOR IF

  • CONDITION PERSISTS OR GET WORSE.

Directions

  • APPLY TO SKIN DIRECTLY OR WITH CLEAN GAUZE, COTTON OR SWAB.
  • FOR RUBBNG, APPLY LIBERALLY AND RUB WITH HANDS.

OTHER INFORMATION

  • DOES NOT CONTAIN, NOR IS INTENDED AS A SUBSTITUTE FOR GRAIN OR ETHYL ALCOHOL
  • KEEP BOTTLE TIGHTLY CLOSED.

Inactive Ingredient

BLUE 1, METHYL SALICYLATE, WATER, YELLOW 5

Rubbing Alcohol_50pct_Wintergreen_12oz

Rubbing Alcohol_50pct_Wintergreen_16oz

RUBBING ALCOHOL  50 PERCENT WITH WINTERGREEN
isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76436-302
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL50 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
METHYL SALICYLATE (UNII: LAV5U5022Y)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76436-302-12355 mL in 1 BOTTLE; Type 0: Not a Combination Product12/03/201411/28/2017
2NDC:76436-302-16475 mL in 1 BOTTLE; Type 0: Not a Combination Product12/03/201411/28/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A12/03/201411/28/2017
Labeler - Viny Health and Beauty Products Inc (963374942)

Revised: 11/2017
Document Id: 52466401-52bd-4ddb-bdcb-cddbc9e73c69
Set id: aaf55ec5-0ee3-4643-af1c-4fb3351bc668
Version: 3
Effective Time: 20171128
 
Viny Health and Beauty Products Inc