Label: REFRESH LACRI-LUBE- mineral oil, petrolatum ointment
- NDC Code(s): 0023-0312-04, 0023-0312-07
- Packager: Allergan, Inc.
- Category: HUMAN OTC DRUG LABEL
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Updated December 1, 2022
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- Active ingredients
For external use only.
To avoid contamination, do not touch tip of container to any surface.
- Replace cap after using.
Stop use and ask a doctor if
you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours.
- For external use only.
- Other information
- Inactive ingredients
- Questions or comments?
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INGREDIENTS AND APPEARANCE
mineral oil, petrolatum ointment
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0023-0312 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINERAL OIL (UNII: T5L8T28FGP) (MINERAL OIL - UNII:T5L8T28FGP) MINERAL OIL 425 mg in 1 g PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 568 mg in 1 g Inactive Ingredients Ingredient Name Strength CHLOROBUTANOL (UNII: HM4YQM8WRC) LANOLIN ALCOHOLS (UNII: 884C3FA9HE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0023-0312-04 1 in 1 CARTON 12/15/1977 1 3.5 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:0023-0312-07 1 in 1 CARTON 12/15/1977 2 7 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part349 12/15/1977 Labeler - Allergan, Inc. (144796497)