Label: ISOPROPYL ALCOHOL 50 PERCENT WINTERGREEN READYINCASE- isopropyl alcohol liquid
- NDC Code(s): 49580-0272-2, 49580-0272-3, 49580-0272-6
- Packager: P & L Development, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 16, 2024
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- Official Label (Printer Friendly)
- Active ingredient (by volume)
- Purpose
- Uses
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Warnings
For external use only
- flammable, keep away from fire or flame
- if taken internally serious gastric disturbances will result
- Directions
- Other information
- Inactive ingredients
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Principal Display Panel
50% Rubbing Alcohol
Isopropyl
wintergreen
first aid antiseptic
Manufactured by:
PL Developments
1874 Hwy 72 W
Clinton, SC 29325
Questions or comments?
Call 1-877-753-3935 Monday-Friday 9AM-5PM EST
WARNING: FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY FOIL UNDER THE CAP IS BROKEN OR MISSING.
FL OZ(mL)
- Package Label
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INGREDIENTS AND APPEARANCE
ISOPROPYL ALCOHOL 50 PERCENT WINTERGREEN READYINCASE
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49580-0272 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 50 mL in 100 mL Inactive Ingredients Ingredient Name Strength FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) METHYL SALICYLATE (UNII: LAV5U5022Y) WATER (UNII: 059QF0KO0R) Product Characteristics Color green Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49580-0272-6 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/30/2014 2 NDC:49580-0272-3 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/30/2014 3 NDC:49580-0272-2 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/30/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 06/30/2014 Labeler - P & L Development, LLC (101896231)