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NDC 70000-0090-02 Lubricant Drops 5 mg/mL Details

Lubricant Drops 5 mg/mL

Lubricant Drops is a OPHTHALMIC SOLUTION/ DROPS in the HUMAN OTC DRUG category. It is labeled and distributed by Cardinal Health, 110 dba LEADER. The primary component is CARBOXYMETHYLCELLULOSE SODIUM.

Product Information

NDC	70000-0090
Product ID	70000-0090_c607e857-ab68-cf66-e053-2a95a90aee36
Associated GPIs	86200010102020
GCN Sequence Number	016278
GCN Sequence Number Description	carboxymethylcellulose sodium DROPS 0.5 % OPHTHALMIC
HIC3	Q6T
HIC3 Description	ARTIFICIAL TEARS
GCN	37381
HICL Sequence Number	003843
HICL Sequence Number Description	CARBOXYMETHYLCELLULOSE SODIUM
Brand/Generic	Generic
Proprietary Name	Lubricant Drops
Proprietary Name Suffix	n/a
Non-Proprietary Name	carboxymethylcellulose sodium
Product Type	HUMAN OTC DRUG
Dosage Form	SOLUTION/ DROPS
Route	OPHTHALMIC
Active Ingredient Strength	5
Active Ingredient Units	mg/mL
Substance Name	CARBOXYMETHYLCELLULOSE SODIUM
Labeler Name	Cardinal Health, 110 dba LEADER
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part349
Listing Certified Through	2022-12-31

Package

Package Images

NDC 70000-0090-02 (70000009002)

Pricing Information
NDC Package Code	70000-0090-2
Billing NDC	70000009002
Package	2 BOTTLE, DROPPER in 1 CARTON (70000-0090-2) / 15 mL in 1 BOTTLE, DROPPER
Marketing Start Date	2021-03-09
NDC Exclude Flag	N
Price Per Unit	0.30222
Pricing Unit	ML
Effective Date	2022-10-19
NDC Description	LUBRICANT 0.5% EYE DROP
Pharmacy Type Indicator	C/I
OTC	Y
Explanation Code	4, 5
Classification for Rate Setting	G
As of Date	2022-11-23

This pricing file, entitled the NADAC (National Average Drug Acquisition Cost) files, provide state Medicaid agencies with covered outpatient drug prices by averaging survey invoice prices from retail community pharmacies across the United States. These pharmacies include independent retail community pharmacies and chain pharmacies. The prices are updated on a weekly and monthly basis

Standard Product Labeling (SPL)/Prescribing Information SPL 1ac2fe24-9ff6-48c1-b123-fbc0e48f5304 Details

Active ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

Eye lubricant

Uses

For the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun.
For use as a protectant against further irritation or to relieve dryness of the eye.

Warnings

For external use only.
To avoid contamination, do not touch tip of container to any surface. Replace cap after using.
If solution changes color or becomes cloudy, do not use.

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.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Instill 1 or 2 drops in the affected eye(s) as needed.

Other information

Use only if imprinted tape seals on top and bottom flaps are intact and clearly legible.
Use before expiration date marked on container.
Discard 90 days after opening
Store at 59°-86°F (15°-30°C).
RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

Boric acid; calcium chloride; magnesium chloride; potassium chloride; purified water; stabilized oxychloro complex; and sodium chloride. May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LUBRICANT DROPS

carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70000-0090
Route of Administration	OPHTHALMIC

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	5 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORITE (UNII: G538EBV4VF)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70000-0090-1	1 in 1 CARTON	03/09/2021
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC:70000-0090-2	2 in 1 CARTON	03/09/2021
2		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part349	03/09/2021

Labeler - Cardinal Health, 110 dba LEADER (063997360)

Revised: 6/2021

Document Id: c607e857-ab68-cf66-e053-2a95a90aee36

Set id: 1ac2fe24-9ff6-48c1-b123-fbc0e48f5304

Version: 3

Effective Time: 20210630