FDA Label for Farewell Collection
View Indications, Usage & Precautions
Farewell Collection Product Label
The following document was submitted to the FDA by the labeler of this product Paveemol Company Limited. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient(S)
Benzalkonium chloride 0.05 %.
Purpose
Antiseptic
Use
To help reduce bacteria on hands.
Warnings
For external use only.
Do Not Use
- in children less than 2 months of age
- on open skin wounds
Otc - 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.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away 1 800-222-1222
Directions
- Apply on hands and leave until full absorption. No rinse is required.
- Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
- Store between 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F)
Inactive Ingredients
aluminum starch octenylsuccinate, beeswax, cetyl alcohol, chlorphenesin, cyclopentasiloxane, C13-14 isoparaffin, ethylhexylglycerin, glycerin, glyceryl stearate, helianthus annuus seed oil, isohexadecane, isopropyl myristate, laureth-7, niacinamide, PEG 100 stearate, phenoxyethanol, purified water USP, propylene glycol, shea butter, sodium polyacrylate, stearyl alcohol, triethylhexanoin, tocopheryl acetate, xanthan gum
Package Label - Principal Display Panel
53 mL NDC : 81892-113-11
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