Label: HAND SANITIZER- alcohol aerosol, spray
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Contains inactivated NDC Code(s)
NDC Code(s): 78358-001-01, 78358-001-02, 78358-001-03 - Packager: Tecnología en Aerosol, S. de R.L. de C.V.
- 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 May 22, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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SPL UNCLASSIFIED SECTION
The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:
Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (70%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
Sodium nitrite (0.09% v/v).
Sodium Benzoate (0.9% v/v).
Dimethylammonium (0.4% v/v)
Morpholine (o.1% v/v)
Triethylene Glycol (6.9% v/v)
Isobutane (28.00% v/v)
Sterile distilled water or boiled cold water.
The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
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WHEN USING
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. If swallowed, get medical help or contact a Poison Control Center right away. - STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HAND SANITIZER
alcohol aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:78358-001 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 TRIETHYLENE GLYCOL (UNII: 3P5SU53360) 6 mL in 100 mL SODIUM NITRITE (UNII: M0KG633D4F) 0.09 mL in 100 mL WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) 0.09 mL in 100 mL 2,4,5-T DIMETHYLAMMONIUM (UNII: OQE98LYN9O) 0.4 mL in 100 mL 2,4-D MORPHOLINE (UNII: 62MSU01E50) 0.1 mL in 100 mL ISOBUTANE (UNII: BXR49TP611) 28 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:78358-001-01 125 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/30/2020 2 NDC:78358-001-02 200 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/30/2020 3 NDC:78358-001-03 500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/30/2020 Labeler - Tecnología en Aerosol, S. de R.L. de C.V. (951578291) Registrant - Tecnología en Aerosol, S. de R.L de C.V. (951578291) Establishment Name Address ID/FEI Business Operations Tecnología en Aerosol S. de R.L. de C.V. 951578291 manufacture(78358-001)
