ROHTO DRY-AID- povidone, propylene glycol liquid

Rohto Dry-Aid by

Drug Labeling and Warnings

Rohto Dry-Aid by is a Otc medication manufactured, distributed, or labeled by The Mentholatum Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Povidone 0.68%

Propylene glycol 0.3%

Purpose

Povidone – Lubricant

Propylene glycol - Lubricant

Uses

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

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
• remove contact lenses before using

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.

Directions

• put 1 or 2 drops in the affected eye(s) as needed
• tightly snap on cap to seal

Other information

• do not freeze

Inactive ingredients

boric acid, calcium chloride, edetate disodium, magnesium sulfate, menthol, PEG-10 castor oil, poloxamer, polyaminopropyl biguanide, polyoxyl stearate, purified water, sesame oil, sodium borate

Questions?

1-877-636-2677 MON-FRI 9AM-5PM (EST)

Principal Display Panel

INGREDIENTS AND APPEARANCE

ROHTO DRY-AID 
povidone, propylene glycol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10742-8162
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) (POVIDONE, UNSPECIFIED - UNII:FZ989GH94E)	POVIDONE, UNSPECIFIED	6.8 mg  in 1 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3)	PROPYLENE GLYCOL	3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
EDETATE DISODIUM (UNII: 7FLD91C86K)
MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)
RACEMENTHOL (UNII: YS08XHA860)
POLYOXYL 35 CASTOR OIL (UNII: 6D4M1DAL6O)
PEG/PPG-105/5 COPOLYMER (UNII: 52901V8XAR)
POLIHEXANIDE HYDROCHLORIDE (UNII: 4XI6112496)
POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
WATER (UNII: 059QF0KO0R)
SESAME OIL (UNII: QX10HYY4QV)
SODIUM BORATE (UNII: 91MBZ8H3QO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10742-8162-1	1 in 1 CARTON	01/01/2017
1		10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC: 10742-8162-2	2 in 1 CARTON	01/01/2017
2		10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	01/01/2017

Labeler - The Mentholatum Company (002105757)