FINEAPPLE Hand Sanitizer
FINEAPPLE Hand Sanitizer is an FDA drug label for the active ingredient ALCOHOL manufactured by CROP BEAUTY GROUP INC. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231026.
Generic: ALCOHOL
Manufacturer: CROP BEAUTY GROUP INC.
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 78768-002
Application: 505G(a)(3)
Effective: 20231026
Active Ingredients: Active ingredient Alcohol 62% Purpose Antiseptic.
Indications & Usage
Use For handwashing to decrease bacteria on the skin.
Dosage & Administration
Directions Wet hands thoroughly with product and allow to dry without wiping.
Contraindications
Not available.
Warnings
Warnings For external use only Flammable, keep away from fire and flame When using this product Avoid the eyes and mucous membranes. In the case of eyes or mucous membranes contact,rinse area thoroughly with water. Stop use and ask a doctor if Condition worsens. Redness or irritation develops. Condition persists for more than 3 days. Keep out of reach of children. If swallowed,contact a doctor or Poison Control Center immediately.
Adverse Reactions
Not available.
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