Label: PLUS RINSE EMERGENCY- purified water liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 72598-011-10, 72598-011-50 - Packager: INNOVATIVE SAFETY SUPPLY INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 October 21, 2022
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
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Directions
- do not dilute solution or reuse bottle
- use only unopened bottle
- to open, twist cap in the direction of the arrow
- avoid contamination of the integrated eyecup
- place integrated eyecup over affected eye(s)
- tilt head backward
- open eyelid(s) wide
- control rate of flow by pressure on bottle
- thoroughly bathe eye(s) with solution
- allow solution to flow away from eye(s)
- rinse until the bottle is empty and continue rinsing with Plum Emergency Eyewash until you reach a doctor
- continue rinsing with water if necessary
- obtain medical treatment.
- Other information
- Inactive ingredients
- Questions or Comments?
- Imported and distributed by
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Principal Display Panel
NDC : 72598-011-50
Plus Rinse
Emergency Eyewash
Compliance: ANSI/ISEA Z358.1-2014
(As Personal Eyewash Only)
Innovative SAFETY SUPPLY
Labeler: Innovative Safety Supply Inc, 368 Edson St, Saskatoon, SK/S7J 0P9/Canada.
www.plusrinse.com
Sterile - 500 ml (16.9 fl oz)
Refill Code: 45961
NDC: 72598-011-10
Plus Rinse
Emergency Eyewash
Compliance: ANSI/ISEA Z358.1-2014
(As Personal Eyewash Only)
Innovative SAFETY SUPPLY
Labeler: Innovative Safety Supply Inc, 368 Edson St, Saskatoon, SK/S7J 0P9/Canada.
www.plusrinse.com
Sterile - 1000 ml (33.8 fl oz)
Refill Code: 45951
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INGREDIENTS AND APPEARANCE
PLUS RINSE EMERGENCY
purified water liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72598-011 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 99.1 mL in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72598-011-50 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/18/2019 2 NDC:72598-011-10 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/18/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part349 06/18/2019 Labeler - INNOVATIVE SAFETY SUPPLY INC. (203168349) Registrant - INNOVATIVE SAFETY SUPPLY INC. (203168349) Establishment Name Address ID/FEI Business Operations Holopack Verpackungstechnik GmbH 343390324 manufacture(72598-011)