Label: HAND SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 78800-002-01, 78800-002-02, 78800-002-03, 78800-002-04, view more78800-002-05, 78800-002-06 - Packager: Octapod, S.A de C.V.
- 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 September 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
- 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
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:78800-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 1.005 mL in 100 mL CARBOMER 1342 (UNII: 809Y72KV36) 0.58 mL in 100 mL WATER (UNII: 059QF0KO0R) TRIETHANOLAMINE HYDRIODIDE (UNII: DT98IT03JK) 0.06 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:78800-002-01 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 2 NDC:78800-002-02 125 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 3 NDC:78800-002-03 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 4 NDC:78800-002-04 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 5 NDC:78800-002-05 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 6 NDC:78800-002-06 3785 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 - Octapod, S.A de C.V. (951578993) Registrant - Octapod, S.A de C.V. (951578993) Establishment Name Address ID/FEI Business Operations Octapod, S.A de C.V. 951578993 manufacture(78800-002) , pack(78800-002) , label(78800-002)
PI 60mL NDC:78800-002-01
PDP 125 mL NDC:78800-002-02
PDP 250 mL NDC:78800-002-03
PDP 500mL NDC:78800-002-04
PDP 1000mL NDC:78800-002-05
PDP 3785 mL NDC:78800-002-06
