Label: DISINFECTANT- disinfectant spray spray
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Contains inactivated NDC Code(s)
NDC Code(s): 80598-001-01, 80598-001-02, 80598-001-03, 80598-001-04, view more80598-001-05, 80598-001-06 - Packager: Aiyinuo Technology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
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 September 24, 2020
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
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Warnings
l.EXTREMELY FLAMMABLE.
Pressurized container; protect from sunlight and don't expose to temperatres exceeding S0°C.Don' t pierce or bum, even after use. Don't spray on a naked flame or any incandescent material. Keep it away from the reach of children. Don't spray towards eyes.
2.External disinfectant shuold not be taken orally and kept out of reach of children.
3.Use with caution if allergic to alcohol.
4.lt should not be used to disinfect fat-soluble surfaces.
5.This product is irritating to wounds and mucous mem-branes. - Do not use
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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Directions
l.Hand disinfection:follow the standard method to use soap to wash hands ,rinse with running water,dry with sterile towels,then direct spray this product on hands and fore-arms until moist wait for 3 minutes,rub hands until dry.
General object surface disinfection: directly spray on the object surface for until moist,wait for 3-Sminutes. - Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
DISINFECTANT
disinfectant spray sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80598-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 75 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALOE (UNII: V5VD430YW9) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80598-001-01 75 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 2 NDC:80598-001-02 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 3 NDC:80598-001-03 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 4 NDC:80598-001-04 160 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 5 NDC:80598-001-05 300 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 6 NDC:80598-001-06 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/30/2020 Labeler - Aiyinuo Technology Co., Ltd. (553901119) Establishment Name Address ID/FEI Business Operations Aiyinuo Technology Co., Ltd. 553901119 manufacture(80598-001)