EYES ALIVE  LUBRICATING- carboxymethylcellulose sodium, unspecified liquid 
RIVIERA PHARMA INC

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Eyes Alive
Lubricating

Drug Facts

Active ingredients

Carboxymethylcellulose sodium 0.5%

Purpose

Eye lubricant

Uses

Warnings

For external use only

Do not use is solution changes color or becomes cloudy.

When using this product

  • to avoid contamination, do not 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 before use 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

Other information

Inactive ingredients

Calcium chloride, hydrochloric acid1, magnesium chloride, potassium chloride, purified water, sodium chloride, sodium hydroxide1, and sodium lactate.


1
May or may not contain this ingredient to adjust pH.

Questions or comments?

800.477.2884, M-F 8AM-5PM Eastern Time

You can always report serious effects to this number.

PRINCIPAL DISPLAY PANEL - 0.6 mL Container Carton

NDC 83291-200-32

Eyes
Alive

Lubricating Eye Drops
Carboxymethylcellulose sodium 0.5%

Preservative Free

IMMEDIATE RELIEF FOR
DRY IRRITATED EYES

32 Sterile Single-Use Containers
0.02 fl oz (0.6 mL) each

MADE IN THE USA

Principal Display Panel - 0.6 mL Container Carton
EYES ALIVE   LUBRICATING
carboxymethylcellulose sodium, unspecified liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83291-200
Route of AdministrationINTRAOCULAR
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83291-200-022 in 1 POUCH06/01/2023
10.6 mL in 1 AMPULE; Type 0: Not a Combination Product
2NDC:83291-200-044 in 1 POUCH06/01/2023
20.6 mL in 1 AMPULE; Type 0: Not a Combination Product
3NDC:83291-200-3232 in 1 CARTON06/01/2023
30.6 mL in 1 AMPULE; Type 0: Not a Combination Product
4NDC:83291-200-5252 in 1 CARTON06/01/2023
40.6 mL in 1 AMPULE; Type 0: Not a Combination Product
5NDC:83291-200-7272 in 1 CARTON06/01/2023
50.6 mL in 1 AMPULE; Type 0: Not a Combination Product
6NDC:83291-200-00100 in 1 CARTON06/01/2023
60.6 mL in 1 AMPULE; Type 0: Not a Combination Product
7NDC:83291-200-088 in 1 CARTON06/01/2023
70.6 mL in 1 AMPULE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01806/01/2023
Labeler - RIVIERA PHARMA INC (118748772)

Revised: 5/2024
Document Id: 7b0dddfc-9933-4f2f-840f-7a7b28cbf1fa
Set id: b6966691-6884-438c-9f89-5924089226e1
Version: 3
Effective Time: 20240531
 
RIVIERA PHARMA INC