Label: HAND SANITIZER CHRISTMAS MEMORIES- isopropyl alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 79883-010-01, 79883-010-02, 79883-010-03, 79883-010-04, view more79883-010-05, 79883-010-06 - 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 25, 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 useon 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 CHRISTMAS MEMORIES
isopropyl alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79883-010 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) CINNAMON OIL (UNII: E5GY4I6YCZ) CLOVE OIL (UNII: 578389D6D0) GINGER OIL (UNII: SAS9Z1SVUK) GLYCERIN (UNII: PDC6A3C0OX) ORANGE OIL (UNII: AKN3KSD11B) VANILLA PLANIFOLIA OIL (UNII: 0A3F415158) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79883-010-01 60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/01/2020 2 NDC:79883-010-02 120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/01/2020 3 NDC:79883-010-03 250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/01/2020 4 NDC:79883-010-04 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/01/2020 5 NDC:79883-010-05 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/01/2020 6 NDC:79883-010-06 120 mL in 1 BOTTLE, PLASTIC; 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) Establishment Name Address ID/FEI Business Operations TAICORP ENTERPRISES LIMITED 202875738 manufacture(79883-010)