NUVALU HAND SANITIZER SWEET PEA 1OZ: Package Insert and Label Information

NUVALU HAND SANITIZER SWEET PEA 1OZ- alcohol gel
Ningbo Liyuan Daily Chemical Products Co.,Ltd.

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.

Ethyl Alcohol 65 percent

Purpose

Antimicrobial

Features

• To decrease bacteria on the skin that could cause disease.
• Recommended for repeated use.
• Use anywhere without water

Directions

• Wet hands thoroughly with product and rub until dry without wiping.
• For children under 6, use only under adult supervision.
• Not recommended for infants.

When using this product

• Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• Do not inhale or ingest.
• Avoid contact with broken skin.

Other information

• Do not store above 105 Fahrenheit
• May discolor some fabrics
• Harmful to wood finishes and plastics

Warnings

• For external use only.
• Flammable. Keep away from heat and flame.
• Discontinue if skin becomes irritated and ask a doctor.
• Keep out of reach of children.
• In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Keep out of reach of children.

Keep out of reach of children.

Inactive Ingredients

Water (aqua), carbomer, fragrance, glycerin, propylene glycol, triethanolamine, tocopheryl acetate (vitamin E), aloe barbadensis leaf juice, FD&C Red No. 40

NUVALU HAND SANITIZER SWEET PEA 1OZ ethyl alcohol gel

Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76176-223 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (ALCOHOL) ALCOHOL 65 mL in 100 mL

Inactive Ingredients Ingredient Name Strength FD&C RED NO. 40 ALOE VERA LEAF PROPYLENE GLYCOL WATER CARBOMER 934 GLYCERIN CUPRIC BIS(TRIETHANOLAMINE) .ALPHA.-TOCOPHEROL ACETATE

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:76176-223-48 29 mL in 1 BOTTLE, PLASTIC None

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 10/01/2019

Labeler — Ningbo Liyuan Daily Chemical Products Co.,Ltd. (530766098)

Registrant — Ningbo Liyuan Daily Chemical Products Co.,Ltd. (530766098)

Establishment
Name	Address	ID/FEI	Operations
Ningbo Liyuan Daily Chemical Products Co., Ltd.		530766098	manufacture (76176-223)

Revised: 10/2019 Ningbo Liyuan Daily Chemical Products Co.,Ltd.