Aloe Vera Gel
FDA Label NDC 47993-220

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Jiangbei Ocean Star Trading Co.,ltd for the product Aloe Vera Gel (NDC 47993-220). 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 otc - active ingredient, otc - purpose, warnings, indications & usage, dosage & administration, otc - keep out of reach of children, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active ingredients--------------purpose

Glycerine..........10%

Propylene Glycol..........4%

Otc - Purpose

Uses:
Keep skin moist. Recommended for repeated use.

Warnings

Warnings:

Keep away from fire or flame.For external use only.Keep out of reach of children.Keep out of reach of eyes.

Indications & Usage

Directions:

Apply small amount in your palm and smear on the skin.

Dosage & Administration

Other Information

Do not store above 110F(43C) May discolor certain fabric or surfaces. Harmful to wood finishes and plastics.


Otc - Keep Out Of Reach Of Children

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

Inactive Ingredient

Inactive Ingredients:

Water,Carbomer,Aloe barbadensis leaf juice power,Edetic acid,Ethoxylated hydrogenated castor oil,Fragrance,Dimethyloldimethy hydantoin,Triethanolamine.

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