Label: SENTIA LUBRICANT EYE DROPS- propylene glycol liquid
- NDC Code(s): 83035-8124-5
- Packager: Singular Dreamer dba True Marker
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 28, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
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Warnings
For external use only
Do not use
- if this product changes color or becomes cloudy
- if you are sensitive to any ingredient in this product
When using this product
- do not touch tip of container to any surface to avoid contamination
- replace cap after each use
Stop use and ask a doctorif you experience any of the
following:- eye pain
- change in vision
- continued redness or irritation of the eye
- condition worsens or persists for more than 72 hours
Keep out of reach of children. If swallowed, get
medical help or contact a Poison Control Center right
away. - KEEP OUT OF REACH OF CHILDREN
- Directions
- Other Information
- Inactive Ingredients
- Questions ?
- Product label
-
INGREDIENTS AND APPEARANCE
SENTIA LUBRICANT EYE DROPS
propylene glycol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83035-8124 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL 0.6 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BORIC ACID (UNII: R57ZHV85D4) POTASSIUM CHLORIDE (UNII: 660YQ98I10) SORBITOL (UNII: 506T60A25R) GLYCERIN (UNII: PDC6A3C0OX) HYALURONIC ACID (UNII: S270N0TRQY) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) BENZETHONIUM CHLORIDE (UNII: PH41D05744) SODIUM CHLORIDE (UNII: 451W47IQ8X) HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83035-8124-5 1 in 1 CARTON 11/27/2023 1 5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M018 11/27/2023 Labeler - Singular Dreamer dba True Marker (129504103) Registrant - Singular Dreamer dba True Marker (129504103)