DOP ISOPROPYL RUBBING ALCOHOL 70%- isopropyl alcohol liquid 
Omega & Delta Co., 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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DOP Isopropyl Rubbing Alcohol 70%

Drug Facts

Active ingredient

Isopropyl alcohol 70%

Purpose

First aid antiseptic

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Use helps prevent the risk of infection in minor cuts, scrapes and burns

Warnings  For external use only

Flammable keep away from fire or flame, heat, spark, electrical

Ask a doctor before use for deep wounds, animal bites or serious burns

When using this product • do not get into eyes • do not apply over large area of the body • do not use longer than 1 week

Stop use and ask a doctor if the condition persists or gets worse

Directions • clean the affected area • apply 1 to 3 times daily

Inactive ingredient Purified water

Other information • does not contain, nor is intended as a substitute for grain or ethyl alcohol • will produce serious gastric disturbances if taken internally

Manufactured by:

Omega & Delta Co., Inc.

Carolina, P.R. 00984

isopropyl alcohol 1

DOP ISOPROPYL RUBBING ALCOHOL 70% 
isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51048-005
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51048-005-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2000
2NDC:51048-005-32946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2000
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/2000
Labeler - Omega & Delta Co., Inc. (090317793)
Establishment
NameAddressID/FEIBusiness Operations
Omega & Delta Co., Inc.090317793manufacture(51048-005)

Revised: 11/2020
Document Id: bd92b199-1ad6-4de9-9dc3-4a349668658d
Set id: c779a35b-1118-4560-8d77-6878edb4c267
Version: 2
Effective Time: 20201112
 
Omega & Delta Co., Inc.