Label: EQUATE SUPPORT ADVANCED LUBRICATING EYE- polyethylene glycol 400 and propylene glycol solution/ drops
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Contains inactivated NDC Code(s)
NDC Code(s): 49035-885-49 - Packager: Wal-Mart Stores, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated April 12, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
- Uses
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Warnings
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For use in the eye(s) only.
- Retain outer carton for full product drug facts.
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
- avoid contamination, do not touch tip of container to any surface.
- replace cap after each use.
- remove contact lenses
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For use in the eye(s) only.
- Directions
- Other information
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Inactive ingredients
Aminomethylpropanol, boric acid, gellan gum, magnesium chloride hexahydrate, potassium chloride, purified water, sodium chloride, sorbitol and Vanish® (stabilized peroxy-complex system as a preservative). May contain hydrochloric acid and/or sodium hydroxide to adjust pH.
Questions?
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
EQUATE SUPPORT ADVANCED LUBRICATING EYE
polyethylene glycol 400 and propylene glycol solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-885 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 400 4 mg in 1 mL PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL 3 mg in 1 mL Inactive Ingredients Ingredient Name Strength AMINOMETHYLPROPANOL (UNII: LU49E6626Q) BORIC ACID (UNII: R57ZHV85D4) GELLAN GUM (LOW ACYL) (UNII: 7593U09I4D) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) POTASSIUM CHLORIDE (UNII: 660YQ98I10) WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) SORBITOL (UNII: 506T60A25R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-885-49 2 in 1 CARTON 06/01/2018 1 0.5 mL in 1 BOTTLE, DROPPER; 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 06/01/2018 Labeler - Wal-Mart Stores, Inc. (051957769) Registrant - Altaire Pharmaceuticals, Inc. (786790378)