Label: GERMY GONE HAND SANITIZER- alcohol gel
-
Contains inactivated NDC Code(s)
NDC Code(s): 79725-001-01, 79725-001-02, 79725-001-03, 79725-001-04, view more79725-001-05, 79725-001-06, 79725-001-07, 79725-001-08, 79725-001-09, 79725-001-10, 79725-001-11 - Packager: GERMY GONE LLC
- Category: HUMAN OTC DRUG LABEL
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 July 9, 2020
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
-
Warnings
For external use only. Flammable. Keep away from heat or flame.
Do not use
- in children less than 2 months of age
- on open skin wounds
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
- Directions
- Other information
- Inactive ingredients
- Product Label
-
INGREDIENTS AND APPEARANCE
GERMY GONE HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79725-001 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 WATER (UNII: 059QF0KO0R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) DENATONIUM BENZOATE (UNII: 4YK5Z54AT2) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S) (UNII: T967IEU43C) TRIISOPROPANOLAMINE (UNII: W9EN9DLM98) LINALOOL, (+)- (UNII: F4VNO44C09) FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK) CUMINYL ACETALDEHYDE (UNII: WSW8QXE6HG) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79725-001-01 18 mL in 1 PACKAGE; Type 0: Not a Combination Product 07/10/2020 2 NDC:79725-001-02 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/10/2020 3 NDC:79725-001-03 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/10/2020 4 NDC:79725-001-04 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/10/2020 5 NDC:79725-001-05 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/10/2020 6 NDC:79725-001-06 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/10/2020 7 NDC:79725-001-07 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/10/2020 8 NDC:79725-001-08 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/10/2020 9 NDC:79725-001-09 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/10/2020 10 NDC:79725-001-10 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/10/2020 11 NDC:79725-001-11 4000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/10/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/10/2020 Labeler - GERMY GONE LLC (117581441)
