Label: LUBRICATING EYE DROPS- carboxymethylcellulose sodium liquid
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NDC Code(s):
73141-001-01,
73141-001-02,
73141-001-03,
73141-001-04, view more73141-001-05
- Packager: A2A Integrated Pharmaceuticals, LLC
- 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 October 7, 2019
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active Ingredient Purpose
- PURPOSE
- Uses
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Warnings
For external use only
• Do not use if solution changes color or becomes cloudy.
When using this product
to avoid contamination, do no touch tip of container to any surface. Do not reuse. Once open, discard.
Do not touch unit dose tip to eye.
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.
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Inactive Ingredients
- Other information
- Principal display panel
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INGREDIENTS AND APPEARANCE
LUBRICATING EYE DROPS
carboxymethylcellulose sodium liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73141-001 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength CALCIUM CHLORIDE (UNII: M4I0D6VV5M) HYDROCHLORIC ACID (UNII: QTT17582CB) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) POTASSIUM CHLORIDE (UNII: 660YQ98I10) WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM HYDROXIDE (UNII: 55X04QC32I) SODIUM LACTATE (UNII: TU7HW0W0QT) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73141-001-01 8 in 1 CARTON 10/04/2019 1 0.6 mL in 1 AMPULE; Type 0: Not a Combination Product 2 NDC:73141-001-02 32 in 1 CARTON 10/04/2019 2 0.6 mL in 1 AMPULE; Type 0: Not a Combination Product 3 NDC:73141-001-03 52 in 1 CARTON 10/04/2019 3 0.6 mL in 1 AMPULE; Type 0: Not a Combination Product 4 NDC:73141-001-04 72 in 1 CARTON 10/04/2019 4 0.6 mL in 1 AMPULE; Type 0: Not a Combination Product 5 NDC:73141-001-05 100 in 1 CARTON 10/04/2019 5 0.6 mL in 1 AMPULE; 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 10/04/2019 Labeler - A2A Integrated Pharmaceuticals, LLC (117064671)