ALOE VESTA- dimethicone lotion

Aloe Vesta by

Drug Labeling and Warnings

Aloe Vesta by is a Otc medication manufactured, distributed, or labeled by Medline Industries, LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Dimethicone 3% w/v

Purpose

Skin protectant

Uses

• temporarily protects and helps relieve chapped or cracked skin and lips
• helps treat and prevent diaper rash
• protects minor skin irritation associated with diaper rash and helps seal out wetness

Warnings

For external use only.

Do not use on

• deep or puncture wounds
• animal bites
• serious burns

When using this product

• do not get into eyes

Stop use and ask a doctor if

• condition worsens
• symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

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

Directions

• for skin protections:
• apply as needed
• for diaper rash:
• change wet and soiled diapers promptly, cleanse the diaper area, and allow to dry
• apply liberally, as often as necessary, with each diaper change, especially at bedtime or any time when exposure to wet diapers may be prolonged

Other information

• store at 15°C-30°C (59°F-86°F)

Inactive ingredients

aloe barbadensis leaf juice, benzyl alcohol, carbomer, cetyl alcohol, glycerin, steareth-2, laureth-23, magnesium aluminum silicate, water, white petrolatum

Manufacturing Information

Manufactured by: Medline Industries, Inc.

Three Lakes Drive, Northfield, IL60093 USA

Made in USA of foreign and domestic materials

www.medline.com

1-800-MEDLINE

REF: 324804

V1RE21GSG

Package Label

INGREDIENTS AND APPEARANCE

ALOE VESTA 
dimethicone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-775
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	30 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER 934 (UNII: Z135WT9208)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
BENZYL ALCOHOL (UNII: LKG8494WBH)
LAURETH-23 (UNII: N72LMW566G)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
STEARETH-2 (UNII: V56DFE46J5)
WHITE PETROLATUM (UNII: B6E5W8RQJ4)
GLYCERIN (UNII: PDC6A3C0OX)
CETYL ALCOHOL (UNII: 936JST6JCN)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53329-775-13	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/01/2021	05/31/2025
2	NDC: 53329-775-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/01/2021	05/31/2025
3	NDC: 53329-775-08	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/01/2021	03/31/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	M016	07/01/2021	05/31/2025

Labeler - Medline Industries, LP (025460908)

Registrant - Medline Industries, LP (025460908)