ALTALUBE- mineral oil and petrolatum ointment 
Altaire Pharmaceuticals Inc.

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Altalube Ointment

ActivEyes

Altalube Ointment 3.5g

NDC 59390-198-50

Drug Facts

Active ingredients

Mineral Oil 15% and White Petrolatum 85%

Purpose

Eye Lubricant

Uses

• as a lubricant to prevent further irritation  • to relieve dryness of the eye(s).

Warnings

• Save box for complete information. • For use in the eyes only.

When using this product

• avoid contamination, do not touch tip of container to any surface.

• replace cap after each use.

Stop use and ask a doctor if

• you experience eye pain, changes in vision, continued redness or irritation of the eye. • condition worsens or persists for more than 72 hours.

Keep this and all drugs out of the reach of children.

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

Directions

• pull down lower lid of the affected eye and apply a small amount (one-fourth inch) of ointment to the inside of the eyelid every 3-4 hours or as directed by a doctor.

Other information

• store at room temperature 15°-30°C (59°-86°F). • protect from freezing.

• see crimp of tube or box for lot number and expiration date.

• keep tightly closed.

• does not contain preservatives.

Inactive Ingredients

None remove

Questions or comments?

• (631) 722-5988• 9AM – 5 PM EST Monday- Friday

PRINCIPAL DISPLAY PANEL

ActiEyes Altalube OintmentWhite Petrolatum and Mineral OilLubricant Eye Ointment Preservative FreeSterileNET WT3.5g (1/8 OZ)







ActiEyes 
Altalube Ointment
White Petrolatum 
and Mineral Oil
Lubricant Eye Ointment 
Preservative Free
Sterile
NET WT
3.5g (1/8 OZ)

ALTALUBE 
mineral oil and petrolatum ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59390-198
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MINERAL OIL (UNII: T5L8T28FGP) (MINERAL OIL - UNII:T5L8T28FGP) MINERAL OIL150 mg  in 1 g
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM850 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
LANOLIN ALCOHOLS (UNII: 884C3FA9HE)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59390-198-501 in 1 CARTON02/01/2002
13.5 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01802/01/2002
Labeler - Altaire Pharmaceuticals Inc. (786790378)
Registrant - Altaire Pharmaceuticals, Inc. (786790378)
Establishment
NameAddressID/FEIBusiness Operations
Altaire Pharmaceuticals, Inc.786790378manufacture(59390-198)

Revised: 12/2023
Document Id: 0c0e9c0d-6205-e63b-e063-6294a90ac0d9
Set id: eb65004c-c3a7-4079-bd75-f2857d30c68a
Version: 4
Effective Time: 20231209
 
Altaire Pharmaceuticals Inc.