NDC 70000-0089 – Dry Eye Relief
Carboxymethylcellulose Sodium, Unspecified 10 mg/mL · Gel · Ophthalmic
Product NDC70000-0089
Product details
- Brand name
- Dry Eye Relief
- Generic name
- Carboxymethylcellulose sodium
- Labeler
- CARDINAL HEALTH 110, LLC. DBA LEADER
- Dosage form
- Gel
- Route
- Ophthalmic
- Marketing category
- OTC MONOGRAPH DRUG · M018
- Marketed since
- March 9, 2021
- Marketing end
- November 30, 2026
Active ingredients
Uses, dosage, side effects and warnings for Dry Eye Relief →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70000-0089-1 | 1 BOTTLE, DROPPER in 1 CARTON (70000-0089-1) / 15 mL in 1 BOTTLE, DROPPER | Mar 9, 2021 |
Recalls mentioning this NDC
- D-0299-2024 Feb 14, 2024 · Class I
Non-Sterility - D-0132-2024 Nov 29, 2023 · Class I
Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.
Other Dry Eye Relief products
- 70000-0088 Polyethylene Glycol 400 4 mg/mL; Propylene Glycol 3 mg/mL · Gel · CARDINAL HEALTH 110, LLC. DBA LEADER
- 59262-803 Glycerin 2.5 mg/mL · Solution/ Drops · Similasan Corporation