Label: RUBBING ALCOHOL 70 PERCENT- isopropyl alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 71611-303-12, 71611-303-16 - Packager: MY Sales LLC dba Click Products LLC
- 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 April 9, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Keep Out of Reach of Children
- WARNINGS
- ASK DOCTOR
- WHEN USING
- STOP USE
- Directions
- OTHER INFORMATION
- Inactive Ingredient
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RUBBING ALCOHOL 70 PERCENT
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71611-303 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:71611-303-16 475 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/22/2018 2 NDC:71611-303-12 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/22/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 02/22/2018 Labeler - MY Sales LLC dba Click Products LLC (080766174)