NDC Code(s) : 37205-763-65
Packager : Cardinal Health

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Leader Lubricating pluscarboxymethylcellulose sodium SOLUTION/ DROPS
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:37205-763
Route of Administration OPHTHALMIC DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Carboxymethylcellulose Sodium(UNII: K679OBS311)
(CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) 		Carboxymethylcellulose Sodium.5 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
CALCIUM CHLORIDE(UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE(UNII: 02F3473H9O)
POTASSIUM CHLORIDE(UNII: 660YQ98I10)
SODIUM CHLORIDE(UNII: 451W47IQ8X)
SODIUM LACTATE(UNII: TU7HW0W0QT)
WATER(UNII: 059QF0KO0R)
SODIUM HYDROXIDE(UNII: 55X04QC32I)
HYDROCHLORIC ACID(UNII: QTT17582CB)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:37205-763-655 in 1 CARTON 26/05/2013
16 in 1 BLISTER PACK
1.4 mL in 1 POUCH 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 05/10/2013

PRINCIPAL DISPLAY PANEL

Compare to Refresh Plus® Lubricant Eye Drops active ingredient

Lubricating PLUS

Carboxymethylcellulose Sodium 0.5%

Lubricant Eye Drops

Moisture Drops for Dry Eyes

Sensitive Preservative-Free

Actual Size

30 STERILE SINGLE-USE CONTAINERS

0.01 FL OZ (0.4 mL) EACH

Leader Lubricating Plus