Label: EQUATE SUPPORT ADVANCED LUBRICANT DROPS MULTIDOSE- polyethylene glycol 400, propylene glycol solution/ drops
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Contains inactivated NDC Code(s)
NDC Code(s): 49035-878-52 - 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 18, 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
- For use in the eyes 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
- do not touch tip of container to any surface avoid contamination.
- remove contact lenses
- replace cap after each use.
- do not deliver more than 6 consecutive drops.
- Directions
- Other information
- Inactive ingredients
- Questions and comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
EQUATE SUPPORT ADVANCED LUBRICANT DROPS MULTIDOSE
polyethylene glycol 400, propylene glycol solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-878 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 4.0 mg in 1 mL PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL 3.0 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) HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-878-52 7.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 06/01/2018 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)