ALOE VESTA- dimethicone lotion 
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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775 Aloe Vesta Daily Moisturizer

Active ingredient

Dimethicone 3% w/v

Purpose

Skin protectant

Uses

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

Other information

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

Aloe Vesta Daily Moisturizer

ALOE VESTA 
dimethicone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-775
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE30 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53329-775-1359 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/202105/31/2025
2NDC:53329-775-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/202105/31/2025
3NDC:53329-775-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/202103/31/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM01607/01/202105/31/2025
Labeler - Medline Industries, LP (025460908)
Registrant - Medline Industries, LP (025460908)

Revised: 8/2023
Document Id: 032195e0-a729-60f4-e063-6394a90a1337
Set id: af5e96dc-6616-5180-e053-2a95a90a6edc
Version: 6
Effective Time: 20230817
 
Medline Industries, LP