Hand Sanitizer 62 mL/100mL
Ethyl Alcohol · SPRAY · UpLift Brands, LLC
Hand Sanitizer is a spray containing ethyl alcohol at 62 mL/100mL, taken topical. Manufactured by UpLift Brands, LLC.
Key Facts
- Brand Name
- Hand Sanitizer
- Generic Name
- Ethyl Alcohol
- NDC Code (Product)
83986-899- Manufacturer
- UpLift Brands, LLC
- Strength
- 62 mL/100mL
- Dosage Form
- SPRAY
- Route
- TOPICAL
- Marketing Status
- Application #
- 505G(a)(3)
- Marketing Start
- 06/06/2016
Recall History
Albek De Mexico S.A. De C.V.
CGMP Deviations: Next Advanced Antibacterial Hand Sanitizer was found to be below the label claim for ethanol content and contained methanol. Other products were recalled because they were manufactured in the same facility as the product found to contain methanol.
SG24 LLC
Marketed without an Approved NDA/ANDA; product labeled to contain 0.56% methanol making it an unapproved new drug
Aroma Release Technologies Inc
Marketed Without an Approved NDA/ANDA: Product labeled to contain methanol making it an unapproved new drug and contains methanol
Fisher Scientific Co., LLC
CGMP Deviations: Voluntary recall of all hand sanitizer distributed after March 31, 2022, due to FDA issued guidance to cease placing hand sanitizer product, produced under temporary approval, into the market after March 31, 2022.
Valisa MFG LLC
Marketed Without an Approved NDA/ANDA: Product labeled to contain methanol making it an unapproved new drug and contains methanol
Real Clean Distribuciones SA de CV
CGMP Deviations: Born Basic Anti Bac was found to be below the label claim for ethanol content and contained methanol. Other products were recalled because they were manufactured in the same facility as the product found to contain methanol.
Scentsational Soaps & Candles Inc
Chemical contamination: product found to be contaminated with methanol (wood alcohol), benzene and acetaldehyde.
Global Sanitizers LLC
Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA (ethyl alcohol 70%) to be below the label claim for ethanol content and to contain methanol.
Global Sanitizers LLC
CGMP Deviations: lots and products of hand sanitizer are being recalled because they were manufactured under the same conditions as the product lot found to contain methanol.
Lula Holdings L.L.C.
CGMP Deviations: FDA analysis found product to contain acetaldehyde above specification limits.
Side Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Full Prescribing Information
Indications & Usage
Uses • Hand sanitizer to help reduce bacteria on the skin that could cause disease • Recommended for repeated use.
Dosage & Administration
Directions • Wet hands thoroughly with product and allow to dry without wiping • For children under 6, do not use without adult supervision •Not recommended for infants.
Warnings
Warnings Highly Flammable. Keep away from fire or flame. For external use only When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Frequently Asked Questions
What is Hand Sanitizer used for?
Hand Sanitizer contains Ethyl Alcohol. It is a spray taken topical. Consult your doctor for specific uses.
Is Hand Sanitizer a controlled substance?
Hand Sanitizer is not classified as a controlled substance by the DEA.
What is the generic name for Hand Sanitizer?
The generic name for Hand Sanitizer is Ethyl Alcohol. There are 12 other brand versions of Ethyl Alcohol.
What is the NDC code for Hand Sanitizer 62 mL/100mL?
The NDC (National Drug Code) for Hand Sanitizer 62 mL/100mL is 83986-899, listed by UpLift Brands, LLC.
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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)