NDC 69994-002

Biolle Gel Tears

Carboxymethylcellulose Sodium, Unspecified Form

Biolle Gel Tears is a Ophthalmic Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Sage Ethnographic Research, Dba Bioll. The primary component is Carboxymethylcellulose Sodium, Unspecified Form.

• Product ID: 69994-002_14537a40-713b-4076-a858-1c5039e720ed
• NDC: 69994-002
• Product Type: Human Otc Drug
• Proprietary Name: Biolle Gel Tears
• Generic Name: Carboxymethylcellulose Sodium, Unspecified Form
• Dosage Form: Solution/ Drops
• Route of Administration: OPHTHALMIC
• Marketing Start Date: 2015-06-01
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part349
• Labeler Name: SAGE Ethnographic Research, dba Bioll
• Substance Name: CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM
• Active Ingredient Strength: 10 mg/mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 69994-002-10

102 VIAL, SINGLE-USE in 1 CARTON (69994-002-10) > .6 mL in 1 VIAL, SINGLE-USE

• Marketing Start Date: 2015-06-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69994-002-32 [69994000232]

Biolle Gel Tears SOLUTION/ DROPS

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part349
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-06-01
• Inactivation Date: 2020-01-31

NDC 69994-002-52 [69994000252]

Biolle Gel Tears SOLUTION/ DROPS

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part349
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-06-01
• Inactivation Date: 2020-01-31

NDC 69994-002-02 [69994000202]

Biolle Gel Tears SOLUTION/ DROPS

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part349
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-06-01
• Inactivation Date: 2020-01-31

NDC 69994-002-72 [69994000272]

Biolle Gel Tears SOLUTION/ DROPS

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part349
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-06-01
• Inactivation Date: 2020-01-31

NDC 69994-002-04 [69994000204]

Biolle Gel Tears SOLUTION/ DROPS

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part349
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-06-01
• Inactivation Date: 2020-01-31

NDC 69994-002-10 [69994000210]

Biolle Gel Tears SOLUTION/ DROPS

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part349
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-06-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM	10 mg/mL

OpenFDA Data

• SPL SET ID: 9f70669f-37eb-4d6f-a8d4-a143835b0290
• Manufacturer:
  • SAGE Ethnographic Research, dba Bioll
• UNII:
  • K679OBS311
• RxNorm Concept Unique ID - RxCUI:
  • 579907

NDC Crossover Matching brand name "Biolle Gel Tears" or generic name "Carboxymethylcellulose Sodium, Unspecified Form"

NDC	Brand Name	Generic Name
69994-002	Biolle Gel Tears	Carboxymethylcellulose Sodium, Unspecified Form
69994-001	Biolle Tears	Carboxymethylcellulose Sodium, Unspecified Form
69183-205	Eyes Alive EYECON	CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM
58790-007	TheraTears Extra	Carboxymethylcellulose Sodium, Unspecified Form
76688-002	TheraTears Extra	Carboxymethylcellulose Sodium, Unspecified Form