Label: LIBERTY HAND SANITIZER GEL- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 73809-8067-1, 73809-8067-2, 73809-8067-3, 73809-8067-4, view more73809-8067-5 - Packager: Surry Chemicals, Inc.
- 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 29, 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
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
LIBERTY HAND SANITIZER GEL
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73809-8067 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 61 L in 100 L Inactive Ingredients Ingredient Name Strength EUCALYPTUS OIL (UNII: 2R04ONI662) 0.0007 L in 100 L CARBOMER 940 (UNII: 4Q93RCW27E) 0.229 L in 100 L GLYCERIN (UNII: PDC6A3C0OX) 1.45 L in 100 L HYDROGEN PEROXIDE (UNII: BBX060AN9V) 0.095 L in 100 L WATER (UNII: 059QF0KO0R) TROLAMINE (UNII: 9O3K93S3TK) 0.0046 L in 100 L Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73809-8067-1 1041 L in 1 CONTAINER; Type 0: Not a Combination Product 04/15/2020 2 NDC:73809-8067-2 208 L in 1 DRUM; Type 0: Not a Combination Product 04/15/2020 3 NDC:73809-8067-3 18.9 L in 1 PAIL; Type 0: Not a Combination Product 04/15/2020 4 NDC:73809-8067-4 3.785 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/15/2020 5 NDC:73809-8067-5 1.89 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/15/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/15/2020 Labeler - Surry Chemicals, Inc. (083630285) Establishment Name Address ID/FEI Business Operations Surry Chemicals, Inc. 083630285 manufacture(73809-8067)