Label: HAND SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 76795-737-01, 76795-737-02, 76795-737-03, 76795-737-04, view more76795-737-05, 76795-737-06, 76795-737-07, 76795-737-09, 76795-737-22, 76795-737-23, 76795-737-25, 76795-737-26, 76795-737-27, 76795-737-28, 76795-737-29 - Packager: PrintJet Corp
- 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 October 6, 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
- 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
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Package Label - Principal Display Panel
118 ML NDC: 76795-737-26
3785 ML NDC: 76795-737-25
473 ML NDC: 76795-737-29
236 ML NDC: 76795-737-28
236 ML NDC: 76795-737-27
118 ML NDC: 76795-737-26
3758 ML NDC: 76795-737-25
60 ML NDC: 76795-737-01
118 ML NDC: 76795-737-02
177 ML NDC: 76795-737-03
237 ML NDC: 76795-737-04
296 ML NDC: 76795-737-09
473 ML NDC: 76795-737-05
946 ML NDC: 76795-737-06
3785 ML NDC: 76795-737-07
3785 ML NDC: 76795-737-22
946 ML NDC: 76795-737-23
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INGREDIENTS AND APPEARANCE
HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76795-737 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 75.225 mL in 100 mL Inactive Ingredients Ingredient Name Strength (2-(((2-(2-AMINO-3-HYDROXY-2-(HYDROXYMETHYL)PROPOXY)-1-HYDROXYPROPYL)HYDROXYPHOSPHORYL)OXY)-1-HYDROXYPROPYL)PHOSPHONIC ACID (UNII: H24O03I2RP) 1.1 mL in 100 mL GLYCERIN (UNII: PDC6A3C0OX) 1.3 mL in 100 mL HYDROGEN PEROXIDE (UNII: BBX060AN9V) 0.125 mL in 100 mL WATER (UNII: 059QF0KO0R) 22.225 mL in 100 mL FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK) 0.025 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76795-737-07 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/26/2020 2 NDC:76795-737-06 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/26/2020 3 NDC:76795-737-01 60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/26/2020 4 NDC:76795-737-02 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/26/2020 5 NDC:76795-737-03 177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/26/2020 6 NDC:76795-737-04 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/26/2020 7 NDC:76795-737-05 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/26/2020 8 NDC:76795-737-09 296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/26/2020 9 NDC:76795-737-22 3785.41 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/26/2020 10 NDC:76795-737-23 946.353 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/26/2020 11 NDC:76795-737-25 3785.41 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/26/2020 12 NDC:76795-737-26 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/26/2020 13 NDC:76795-737-27 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/26/2020 14 NDC:76795-737-28 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/26/2020 15 NDC:76795-737-29 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/26/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/26/2020 Labeler - PrintJet Corp (158605449) Registrant - Sue Sotelo (158605449) Establishment Name Address ID/FEI Business Operations PrintJet Corp 158605449 manufacture(76795-737)