Label: HAND SANITIZER LEMONGRASS- isopropyl alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 79883-002-01, 79883-002-02, 79883-002-03, 79883-002-05 - Packager: Taicorp Enterprises Limited
- 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 August 2, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
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Warnings
For external use only.
Flammability warning: Keep away from heat or flame.
Do not use
on children less than 2 years of age (unless directed by a doctor).When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Stop use and consult a doctor if irritation develops.
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
HAND SANITIZER LEMONGRASS
isopropyl alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79883-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WEST INDIAN LEMONGRASS OIL (UNII: 5BIA40E9ED) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79883-002-01 120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/01/2020 2 NDC:79883-002-02 250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/01/2020 3 NDC:79883-002-03 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/01/2020 4 NDC:79883-002-05 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/01/2020 Labeler - Taicorp Enterprises Limited (202875738)