Aloe Vesta

Manufacturer: Medline Industries, LP
Effective date: 2023-08-17
Label type: HUMAN OTC DRUG LABEL
Version: 6
Source: legacy-cache
Hydrated at: 2026-08-01 21:27:14

Label at a glance#

ProductAloe Vesta

Active ingredientDIMETHICONE

Label structure9 sections

Indications and 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

Dosage and administration

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

Contacts and useful links#

Websitewww.medline.com

www.medline.com

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Dimethicone 3% w/v

Purpose

OTC - PURPOSE SECTION

Skin protectant

Uses

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

For external use only.

Do not use on

OTC - DO NOT USE SECTION

deep or puncture wounds
animal bites
serious burns

When using this product

OTC - WHEN USING SECTION

do not get into eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

OTHER SAFETY INFORMATION

store at 15°C-30°C (59°F-86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Manufacturing Information

SPL UNCLASSIFIED SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aloe Vesta Daily Moisturizer

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
53329-775-04	2023-08-08	C162847	48780-1	0191ceaa-682a-198a-e063-dbdaa90aec3e	775 Aloe Vesta Daily Moisturizer
53329-775-08	2023-08-08	C162847	48780-1	0191ceaa-682a-198a-e063-dbdaa90aec3e	775 Aloe Vesta Daily Moisturizer
53329-775-13	2023-08-08	C162847	48780-1	0191ceaa-682a-198a-e063-dbdaa90aec3e	775 Aloe Vesta Daily Moisturizer
53329-775-04	2023-07-28	C162847	48780-1	0191ceaa-682a-198a-e063-dbdaa90aec3e	775 Aloe Vesta Daily Moisturizer
53329-775-08	2023-07-28	C162847	48780-1	0191ceaa-682a-198a-e063-dbdaa90aec3e	775 Aloe Vesta Daily Moisturizer
53329-775-13	2023-07-28	C162847	48780-1	0191ceaa-682a-198a-e063-dbdaa90aec3e	775 Aloe Vesta Daily Moisturizer

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
53329-775	ALOE VESTA (DIMETHICONE) LOTION [MEDLINE INDUSTRIES, LP]	6	Legacy NDC	20230818_af5e96dc-6616-5180-e053-2a95a90a6edc.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

Aloe Vesta
dimethicone
CARBOMER 934
SODIUM HYDROXIDE
BENZYL ALCOHOL
LAURETH-23
MAGNESIUM ALUMINUM SILICATE
STEARETH-2
WHITE PETROLATUM
GLYCERIN
CETYL ALCOHOL
ALOE VERA LEAF
POTASSIUM SORBATE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
53329-775	53329-775-13, 53329-775-04, 53329-775-08

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CARBOMER 934	Z135WT9208	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
BENZYL ALCOHOL	LKG8494WBH	IACT
LAURETH-23	N72LMW566G	IACT
DIMETHICONE	92RU3N3Y1O	ACTIB
MAGNESIUM ALUMINUM SILICATE	6M3P64V0NC	IACT
STEARETH-2	V56DFE46J5	IACT
WHITE PETROLATUM	B6E5W8RQJ4	IACT
GLYCERIN	PDC6A3C0OX	IACT
CETYL ALCOHOL	936JST6JCN	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
POTASSIUM SORBATE	1VPU26JZZ4	IACT
WATER	059QF0KO0R	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
032195e0-a729-60f4-e063-6394a90a1337			af5e96dc-6616-5180-e053-2a95a90a6edc	2023-08-17	Warnings	Exact identifier spl id: 032195e0-a729-60f4-e063-6394a90a1337 spl set id: af5e96dc-6616-5180-e053-2a95a90a6edc

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.