Label: ISOPROPYL ALCOHOL liquid
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NDC Code(s):
0869-0810-08,
0869-0810-43,
0869-0810-45,
0869-0810-72, view more0869-0810-99
- Packager: Vi-Jon, 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 January 20, 2023
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
- Warnings
- Ask a doctor before use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
- Caution
- Directions
- other information
- inactive ingredient
- SPL UNCLASSIFIED SECTION
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principal display panel
NDC 0869-0810-45
SWAN
70% Isopropyl Alcohol
- First Aid Antseptic
- For Rubbing & Massaging
Square bottle uses less plastic than a similarly sized bottle Recyclable (if available in your area)
WARNING FLAMMABLE-Keep away from heat, spark, electrical fire or flame
CAUTION: Do not point at self or other; product will squirt when squeezed.
Use only in a well-ventilated area: fumes can be harmful
32 FL OZ (1 QT) 946 mL
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principal display panel
mountain falls
body rub
for treatment of minor cuts and abrasions
topical antiseptic & sanitizer
massage
70% isopropyl alcool
first aid antiseptic
WARNING FLAMMABLE - Keep away from heat, spark, electrical, fire or flame
Use only in a well-ventilated area; fumes can be harmful
Caution: Do not point at self or others; product will squirt when squeezed.
32 FL OZ (1 QT) 946 mL
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INGREDIENTS AND APPEARANCE
ISOPROPYL ALCOHOL
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0869-0810 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:0869-0810-43 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/1989 2 NDC:0869-0810-45 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/1989 3 NDC:0869-0810-08 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/1989 4 NDC:0869-0810-99 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/1989 5 NDC:0869-0810-72 295 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/09/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/15/1989 Labeler - Vi-Jon, LLC (790752542) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(0869-0810) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(0869-0810)