Active Ingredient(S)
Alcohol denat 62%
The following Structured Product Label (SPL) was submitted to the FDA by Landy International for the product Hand Sanitizer (NDC 51706-964). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Alcohol denat 62%
Antiseptic
for hadwashing to decrease bacteria on the skin
For external use only. Flammable. Keep away from heat or flame
dose not contain grain alcohol,do not drink,if taken internally will produce serious gastric distubances.
When using this product
avoid contact with eyes,if contact occurs,flush eyes with water
avoid contact with broken skin
Stop use and ask a doctor if condition worsens
redness or irrtation develops
contidion persists fro more than 3 days
Keep out of reach of children.
in case of accidental ingestion ,seek professinal assistance or contact a Poison Control Center immediately.
Store at 68° to 77F(20° to 25°c).
Do not store above 105°.
May discolor some fabrics.
Not recommended for infants.
Harmful to wood finishes and
plastics.
Water(Aqua), Glycerin, Carbome,Triethanolamine, Fragrance(Parfum),Lactose,
Cellulose, Hydroxypropyl Methylcellulose,Jojoba Estes, locopheryl Acetate, Ascorbyl,Palmitate, Ultramarines(CI 77007),
D&C Red NO.33(CI 17200),FD&C YVellow No.5(Cl 19140).
30 mL WMCA20S021-1 NDC: 51706-964-01
30 mL WMCA20S039 NDC: 51706-964-02
30 mL WST21A066 NDC: 51706-964-03
30 mL WST21A070R NDC: 51706-964-04
30 mL WST21A065B NDC: 51706-964-05
30 mL WST21A065P NDC: 51706-964-06
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