Naturall MOISTURIZING Hand Sanitizer: Package Insert and Label Information

NATURALL MOISTURIZING HAND SANITIZER- alcohol gel
Solv-All Alliance Group, LLC

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.

Drug Facts

Active ingredient[s]

Alcohol 70% v/v

Purpose

Antiseptic

Use[s]

Hand and surface sanitizer to help reduce bacteria that potentially can cause disease.

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do not use

• on children less than 2 months of age

• on open skin wounds

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.

Directions

• Apply enough product to hands and surface area. Rub hands together. Let air dry.

• 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

Glycerin, PEG-6 (and) AMP-Acrylates/Vinyl Isodecanoate Crosspolymer, Purified Water USP

Packaging

IMAGE
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NATURALL MOISTURIZING HAND SANITIZER
alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:77023-070
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 70 mL in 100 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
POLYETHYLENE GLYCOL 300
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%)
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:77023-070-01 3780 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 09/22/2020
Labeler — Solv-All Alliance Group, LLC (115223329)

Revised: 10/2020 Solv-All Alliance Group, LLC

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