Label: ISOPROPYL RUBBING ALCOHOL 70% WITH WINTERGREEN- isopropyl alcohol liquid
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NDC Code(s):
52000-011-01,
52000-011-02,
52000-011-03,
52000-011-04, view more52000-011-05, 52000-011-06, 52000-011-07
- Packager: Universal Distribution Center LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 17, 2024
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- SPL UNCLASSIFIED SECTION
- INACTIVE INGREDIENT
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ISOPROPYL RUBBING ALCOHOL 70% WITH WINTERGREEN
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52000-011 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) METHYL SALICYLATE (UNII: LAV5U5022Y) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52000-011-01 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/15/2012 2 NDC:52000-011-02 177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/15/2012 3 NDC:52000-011-03 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/15/2012 4 NDC:52000-011-04 296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/15/2012 5 NDC:52000-011-05 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/15/2012 6 NDC:52000-011-06 414 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/15/2012 7 NDC:52000-011-07 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/15/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 03/15/2012 Labeler - Universal Distribution Center LLC (019180459) Registrant - Universal Distribution Center LLC (019180459)