Label: DOP ISOPROPYL RUBBING ALCOHOL 70%- isopropyl alcohol liquid
- NDC Code(s): 51048-005-16, 51048-005-32
- Packager: Omega & Delta Co., Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated November 12, 2020
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- Drug Facts
- Active ingredient
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- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
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
- DOSAGE & ADMINISTRATION
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INGREDIENTS AND APPEARANCE
DOP ISOPROPYL RUBBING ALCOHOL 70%
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51048-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51048-005-16 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/01/2000 2 NDC:51048-005-32 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/01/2000 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/01/2000 Labeler - Omega & Delta Co., Inc. (090317793) Establishment Name Address ID/FEI Business Operations Omega & Delta Co., Inc. 090317793 manufacture(51048-005)