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Lantiseptic Protective

Dosage form: ointment
Ingredients: PETROLATUM 430mg in 1mL
Labeler: Santus LLC
NDC Code: 12090-0083

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.

Lantiseptic Protective Ointment

Drug Facts

Active Ingredient

Petrolatum 43%

Purpose

Skin Protectant

Uses

• Temporarily protects minor cuts, scrapes and burns. • Temporarily protects and helps relieve chafed, chapped or cracked skin and lips. • Helps treat and prevent incontinence associated dermatitis.

Warnings

• For external use only.

Do not use

on deep or puncture wounds, animal bites and serious burns.

When using this product

do not get into eyes.

Stop use and see a doctor

if condition lasts more than 7 days.

Keep out of reach of children.

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

Directions

• Gently cleanse and dry area. • Apply liberally to affected area as needed.

Other Information

Store at 15-30° C (59-86°F)

Inactive Ingredients

Aloe Vera Gel, Beeswax, Disodium EDTA, DMDM Hydantoin + IPBC, Glycerin, Lanolin, Lanolin Alcohol, Mineral Oil, Purified Water, Sodium Borate, Sorbitan Sesquioleate.

Questions or Comments?

844-7SANTUS or visit www.lantiseptic.com

Package Labeling:

LANTISEPTIC PROTECTIVE 
petrolatum ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12090-0083
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PETROLATUM (PETROLATUM) PETROLATUM430 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF 
YELLOW WAX 
EDETATE DISODIUM 
GLYCERIN 
LANOLIN 
LANOLIN ALCOHOLS 
MINERAL OIL 
WATER 
SODIUM BORATE 
SORBITAN SESQUIOLEATE 
Packaging
#Item CodePackage Description
1NDC:12090-0083-11 TUBE in 1 CARTON
1250 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34703/30/2016
Labeler - Santus LLC (079868223)

Revised: 01/2017
 
Santus LLC

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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