Label: 75% ALCOHOL SANITIZER- 75% alcohol sanitizer spray spray
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Contains inactivated NDC Code(s)
NDC Code(s): 78792-011-01, 78792-011-02, 78792-011-03, 78792-011-04 - Packager: GUANGDONG THEAOSON TECHNOLOGY 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 15, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
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Use
1.Can be sprayed on cotton ball or tissue paper for local disinfection.
2.Can be directly sprayed on the intact surface of the human body for disinfection.
3.For general objects, disinfection and spraying can be performed for 2-3 seconds.
Larger space disinfection will increase the spraying time accordingly.
4.After spraying, wait 2-3 minutes for best result. - Warnings
- Do not use
- WHEN USING
- 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
75% ALCOHOL SANITIZER
75% alcohol sanitizer spray sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:78792-011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 75 g in 100 g Inactive Ingredients Ingredient Name Strength BUTANE (UNII: 6LV4FOR43R) WATER (UNII: 059QF0KO0R) PROPANE (UNII: T75W9911L6) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:78792-011-01 75 g in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 2 NDC:78792-011-03 140 g in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 3 NDC:78792-011-04 270 g in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 4 NDC:78792-011-02 125 g 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 - GUANGDONG THEAOSON TECHNOLOGY CO.,LTD (560428126) Registrant - GUANGDONG THEAOSON TECHNOLOGY CO.,LTD (560428126) Establishment Name Address ID/FEI Business Operations GUANGDONG THEAOSON TECHNOLOGY CO.,LTD 560428126 manufacture(78792-011)