OTC Medication Information: 2PK 2OZ HAND SANITIIZER-ALOE VERA

2PK 2OZ HAND SANITIIZER-ALOE VERA- alcohol liquid
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.

Active Ingredient

Ethyl Alcohol 62.0%

Purpose

Antimicrobial

Uses

Hand Sanitizer to help reduce bacteria on skin.

Warnings

Flammable. Keep away from hear or flame.

For external use only.

Directions

Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.

Children under 6 years of age should be supervised when using this product.

Keep out of reach of Children.

Children under 6 years of age should be supervised when using this product.

INACTIVE INGREDIENTS

Water (Aqua), Aloe Barbadensis Leaf Juice, Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), Triethanolamine, FD&C Blue No.1, FD&C Yellow No 5.

When using this product

When using this product: Do not use in or near the eyes. In case of contact, rinse eyes thoroughtly with water. Stop use and ask doctor if irritation or rash appears and lasts. Keep out of reach for children.

If swallowed, get medical help or contact a Poison Control Center right away.

Other Information

Store below 106℉. (41℃)

May discolor certain fabrics or surfaces

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2PK 2OZ HAND SANITIIZER-ALOE VERA
2oz hand sanitizer liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:76176-031
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 62 mL
Inactive Ingredients
Ingredient Name Strength
WATER 36 mL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:76176-031-01 1 LIQUID 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 04/01/2017
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 (76176-031)

Revised: 12/2017 Ningbo Liyuan Daily Chemical Products Co., Ltd.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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