773 Aloe Vesta Skin Protectant Ointment

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]

ALOE VESTA- petrolatum ointment 
Medline Industries, LP

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.

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773 Aloe Vesta Skin Protectant Ointment

Active ingredient

White petrolatum 43% w/w

Purpose

Skin protectant

Uses

• temporarily protects minor cuts, scrapes, burns
• temporarily protects and helps relieve chapped or cracked skin and lips

Warnings

For external use only.

Do not use on

• deep or puncture wounds
• animal bites
• serious burns

When using this product

do not get in 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

• apply as needed

Other information

• storage conditions: store at 59°F-86°F (15°C-30°C)

Inactive ingredients

aloe barbadensis leaf juice, DMDM hydantoin, glycerin, hydroxylated lanolin, iodopropynyl butylcarbamate, magnesium sulfate, mineral oil, ozokerite wax, PEG-30 dipolyhydroxystearate, sorbitan sesquioleate, steareth-20, water

Manufacturing Information

Manufacture for Medline Industries, LP

Three Lakes Drive, Northfield, IL 60093 USA

Made in USA with foreign and domestic materials

www.medline.com

1-800-MEDLINE

REF: 324908

V1 RE21AXQ

Package Label

ALOE VESTA 
petrolatum ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-773
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	43 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)
DMDM HYDANTOIN (UNII: BYR0546TOW)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
MINERAL OIL (UNII: T5L8T28FGP)
WATER (UNII: 059QF0KO0R)
STEARETH-20 (UNII: L0Q8IK9E08)
CERESIN (UNII: Q1LS2UJO3A)
HYDROXYLATED LANOLIN (UNII: EOI0B9800C)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53329-773-14	56 g in 1 TUBE; Type 0: Not a Combination Product	09/30/2020	06/30/2025
2	NDC: 53329-773-18	226 g in 1 TUBE; Type 0: Not a Combination Product	09/30/2020	08/31/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	M016	09/30/2020	08/31/2025

Labeler - Medline Industries, LP (025460908)

Registrant - Medline Industries, LP (025460908)

Revised: 8/2023

Document Id: 03c3925a-c812-6731-e063-6294a90a5939

34390-5

Set id: af5f267c-c208-83d8-e053-2a95a90a9dc9

Version: 4

Effective Time: 20230825