Drugplain

Rohto Dry-Aid 6.8 mg/mL

povidone, propylene glycol · LIQUID · The Mentholatum Company

No Recall History
Plain English

Rohto Dry-Aid is a liquid containing povidone, propylene glycol at 6.8 mg/mL, taken ophthalmic. Manufactured by The Mentholatum Company.

Key Facts

Brand Name
Rohto Dry-Aid
Generic Name
povidone, propylene glycol
NDC Code (Product)
10742-8162
Manufacturer
The Mentholatum Company
Strength
6.8 mg/mL
Dosage Form
LIQUID
Route
OPHTHALMIC
Marketing Status
Application #
M018
Marketing Start
01/01/2017

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses temporarily relieves burning and irritation due to dryness of the eye protects against further irritation or to relieve dryness of the eye

Dosage & Administration

Directions put 1 or 2 drops in the affected eye(s) as needed tightly snap on cap to seal Other information do not freeze

Warnings

Warnings For external use only When using this product do not touch tip of container to any surface to avoid contamination replace cap after each use do not use if solution changes color or becomes cloudy Stop use and ask a doctor if you feel eye pain changes in vision occur redness or irritation of the eyes lasts condition worsens or lasts more than 72 hours Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Frequently Asked Questions

What is Rohto Dry-Aid used for?

Rohto Dry-Aid contains povidone, propylene glycol. It is a liquid taken ophthalmic. Consult your doctor for specific uses.

Is Rohto Dry-Aid a controlled substance?

Rohto Dry-Aid is not classified as a controlled substance by the DEA.

What is the generic name for Rohto Dry-Aid?

The generic name for Rohto Dry-Aid is povidone, propylene glycol. There are 1 other brand versions of povidone, propylene glycol.

What is the NDC code for Rohto Dry-Aid 6.8 mg/mL?

The NDC (National Drug Code) for Rohto Dry-Aid 6.8 mg/mL is 10742-8162, listed by The Mentholatum Company.

Product NDC

10742-8162

Package NDC

10742-8162-1

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)