ISOPROPYL ALCOHOL 50 PERCENT WINTERGREEN READYINCASE- isopropyl alcohol liquid 
P & L Development, LLC

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Drug Facts

Active ingredient (by volume)

Isopropyl alcohol (50% conc.)

Purpose

first aid antiseptic

Uses

Warnings

For external use only

Ask a doctor before use if you have

  • deep or puncture wounds, animal bites or serious burns

When using this product

  • do not get into eyes
  • do not apply over large areas of the body
  • do not use longer than one week unless directed by a doctor
  • do not use other than as directed

Stop use and ask a doctor if

  • condition persists or gets worse

Keep out of reach of children.

In case of ingestion, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Directions

Other information

Inactive ingredients

FD&C green #3, FD&C yellow #5, methyl salicylate, purified water

Principal Display Panel

50% Rubbing Alcohol

Isopropyl

wintergreen

first aid antiseptic

Manufactured by:

PL Developments

1874 Hwy 72 W

Clinton, SC 29325

Questions or comments?

Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

WARNING: FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY FOIL UNDER THE CAP IS BROKEN OR MISSING.

FL OZ(mL)

Package Label

Isopropyl Alcohol (50% conc.)

READYinCASE 50% Rubbing Alcohol Wintergreen

ISOPROPYL ALCOHOL  50 PERCENT WINTERGREEN READYINCASE
isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49580-0272
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
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
METHYL SALICYLATE (UNII: LAV5U5022Y)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
ColorgreenScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49580-0272-6473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/30/2014
2NDC:49580-0272-3946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/30/2014
3NDC:49580-0272-2355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/30/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00306/30/2014
Labeler - P & L Development, LLC (101896231)

Revised: 1/2024
Document Id: 31433594-2b7f-4139-8a30-62991963694c
Set id: f9ff67b0-c4ad-4162-b3ef-27a85ed0da25
Version: 9
Effective Time: 20240116
 
P & L Development, LLC