Label: BEE WELL HAND SANITIZER- isopropyl alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 80655-420-69 - Packager: Bee Well LLC
- 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)
- Drug Facts
- Active Ingredient(s)
- Purpose
- Use(s)
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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.
- Directions
- Other information
- INACTIVE INGREDIENT
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SPL UNCLASSIFIED SECTION
Natural Skincare
GERANIUM-EUCALYPTUS
Made in Flagstaff, Arizona, Bee Well hand sanitizer is a geranium-eucalyptus sanitizer spray made with organic essential oils and isopropyl alcohol. Our hygienic sanitizer is great for use where water is limited, on hands, surfaces, and in public spaces. We believe we can only truly grow if we contribute to the health and safety of all, Bee Well is committed to dedicating profits to local mutual aid groups and communities impacted by the current health crisis.
DISTRIBUTED BY: Bee Well. Flagstaff,
Arizona 86001 USA
www.beewell.care | MADE IN USA
- Packaging
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INGREDIENTS AND APPEARANCE
BEE WELL HAND SANITIZER
isopropyl alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80655-420 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 WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) HYDROGEN PEROXIDE (UNII: BBX060AN9V) GERANIUM OIL, ALGERIAN TYPE (UNII: 5Q1I94P4WG) EUCALYPTUS OIL (UNII: 2R04ONI662) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80655-420-69 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/10/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/10/2020 Labeler - Bee Well LLC (117534705) Establishment Name Address ID/FEI Business Operations Bee Well LLC 117534705 manufacture(80655-420)
