Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Rabin Bista, M.B.B.S. [2]
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NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Carboxymethyl cellulose is a Ophthalmologic Agent that is FDA approved for the treatment of burning, irritation and discomfort due to dryness of the eye. Common adverse reactions include eye pain, changes in vision, irritation of the eye.
There is limited information regarding Off-Label Guideline-Supported Use of Carboxymethyl cellulose in adult patients.
There is limited information regarding Off-Label Non–Guideline-Supported Use of Carboxymethyl cellulose in adult patients.
There is limited information regarding FDA-Labeled Use of Carboxymethyl cellulose in pediatric patients.
There is limited information regarding Off-Label Guideline-Supported Use of Carboxymethyl cellulose in pediatric patients.
There is limited information regarding Off-Label Non–Guideline-Supported Use of Carboxymethyl cellulose in pediatric patients.
There is limited information regarding Carboxymethyl cellulose Contraindications in the drug label.
There is limited information regarding Postmarketing Experience of Carboxymethyl cellulose in the drug label.
There is limited information regarding Carboxymethyl cellulose Drug Interactions in the drug label.
There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Carboxymethyl cellulose in women who are pregnant.
There is no FDA guidance on use of Carboxymethyl cellulose during labor and delivery.
There is no FDA guidance on the use of Carboxymethyl cellulose with respect to nursing mothers.
There is no FDA guidance on the use of Carboxymethyl cellulose with respect to pediatric patients.
There is no FDA guidance on the use of Carboxymethyl cellulose with respect to geriatric patients.
There is no FDA guidance on the use of Carboxymethyl cellulose with respect to specific gender populations.
There is no FDA guidance on the use of Carboxymethyl cellulose with respect to specific racial populations.
There is no FDA guidance on the use of Carboxymethyl cellulose in patients with renal impairment.
There is no FDA guidance on the use of Carboxymethyl cellulose in patients with hepatic impairment.
There is no FDA guidance on the use of Carboxymethyl cellulose in women of reproductive potentials and males.
There is no FDA guidance one the use of Carboxymethyl cellulose in patients who are immunocompromised.
There is limited information regarding Monitoring of Carboxymethyl cellulose in the drug label.
There is limited information regarding IV Compatibility of Carboxymethyl cellulose in the drug label.
There is limited information regarding Overdose of Carboxymethyl cellulose in the drug label.
There is limited information regarding Carboxymethyl cellulose Mechanism of Action in the drug label.
There is limited information regarding Pharmacodynamics of Carboxymethyl cellulose in the drug label.
There is limited information regarding Pharmacokinetics of Carboxymethyl cellulose in the drug label.
There is limited information regarding Nonclinical Toxicology of Carboxymethyl cellulose in the drug label.
There is limited information regarding Clinical Studies of Carboxymethyl cellulose in the drug label.
There is limited information regarding Carboxymethyl cellulose Storage in the drug label.
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There is limited information regarding Patient Counseling Information of Carboxymethyl cellulose in the drug label.
There is limited information regarding Carboxymethyl cellulose Look-Alike Drug Names in the drug label.
The contents of this FDA label are provided by the National Library of Medicine.