Label: NON-WASH DISINFECTANT- alcohol liquid
NON-WASH SANITISERGEL- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 74457-101-01, 74457-101-02, 74457-101-03, 74457-101-04, view more74457-101-05, 74457-101-06, 74457-101-07, 74457-101-08, 74457-101-09, 74457-101-10, 74457-101-11, 74457-201-01, 74457-201-02, 74457-201-03, 74457-201-04, 74457-201-05, 74457-201-06, 74457-201-07, 74457-201-08, 74457-201-09, 74457-201-10, 74457-201-11 - Packager: Shera Heman Zhejiang Biotechnologies Co.,Ltd.
- 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 December 23, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
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WHEN USING
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. - STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
NON-WASH DISINFECTANT
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74457-101 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 WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74457-101-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 2 NDC:74457-101-02 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 3 NDC:74457-101-03 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 4 NDC:74457-101-04 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 5 NDC:74457-101-05 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 6 NDC:74457-101-06 300 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 7 NDC:74457-101-07 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 8 NDC:74457-101-08 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 9 NDC:74457-101-09 4000 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 10 NDC:74457-101-10 5000 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 11 NDC:74457-101-11 25000 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 12/24/2020 NON-WASH SANITISERGEL
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74457-201 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 WATER (UNII: 059QF0KO0R) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74457-201-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 2 NDC:74457-201-02 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 3 NDC:74457-201-03 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 4 NDC:74457-201-04 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 5 NDC:74457-201-05 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 6 NDC:74457-201-06 300 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 7 NDC:74457-201-07 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 8 NDC:74457-201-08 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 9 NDC:74457-201-09 4000 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 10 NDC:74457-201-10 5000 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 11 NDC:74457-201-11 25000 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/24/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 12/24/2020 Labeler - Shera Heman Zhejiang Biotechnologies Co.,Ltd. (554528847) Establishment Name Address ID/FEI Business Operations Shera Heman Zhejiang Biotechnologies Co.,Ltd. 554528847 manufacture(74457-101, 74457-201)