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Drug Facts
Raggedy Ann And Andy Foam
FDA Label NDC 75878-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by My Habitat Brands Llc for the product Raggedy Ann And Andy Foam (NDC 75878-003). 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 other, active ingredient, purpose, uses, otc - 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.
Label Section Quick Index
Active Ingredient
Benzalkonium Chloride 0.13%
Purpose
Antibacterial
Uses
- For hand washing and to decrease bacteria on the skin.
- Recommended for repeated use.
Otc - Do Not Use
- For external use only.
Otc - When Using
When using this product, keep out of eyes. In case of contact with eyes, immediately flush eyes with water. Avoid contact with broken skin.
Otc - Stop Use
Discontinue use if irritation or redness develops. If condition persists for more than 72 hours consult a doctor.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.
Directions
- Wet hands. Apply palm full to hands. Scrub thoroughly. Rinse. Recommended for repeated use.
Inactive Ingredients
Water, Cocamidopropyl Betaine, Glycerin, Fragrance, Citric Acid, Disodium EDTA, Tocopheryl Acetate, FD&C Yellow No.5
Principal Display Panel - 221Ml Bottle Label
Raggedy
Ann&Andy™
ANTIBACTERIAL
FORMULA Enriched
with Vitamin E
FOAM HAND SOAP
Vanilla
Bean
7.5 FL OZ (221ml)
Principal Display Panel (221ml Bottle Label)
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