ROHTO JOLT- hypromellose liquid

Land: USA

Språk: engelska

Källa: NLM (National Library of Medicine)

Aktiva substanser:

HYPROMELLOSE 2906 (4000 MPA.S) (UNII: 5EYA69XGAT) (HYPROMELLOSE 2906 (4000 MPA.S) - UNII:5EYA69XGAT)

Tillgänglig från:

The Mentholatum Company

Administreringssätt:

OPHTHALMIC

Receptbelagda typ:

OTC DRUG

Terapeutiska indikationer:

Hypromellose - Lubricant

Bemyndigande status:

OTC monograph final

Produktens egenskaper

ROHTO JOLT- HYPROMELLOSE LIQUID
THE MENTHOLATUM COMPANY
_Disclaimer: Most OTC drugs are not reviewed and approved by FDA,
however they may be marketed if they_
_comply with applicable regulations and policies. FDA has not
evaluated whether this product complies._
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DRUG FACTS
ACTIVE INGREDIENT
Hypromellose 0.35%
PURPOS E
Hypromellose - Lubricant
US ES
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•
WARNINGS
FOR EXTERNAL USE ONLY
WHEN USING THIS PRODUCT
•
•
•
•
STOP USE AND ASK A DOCTOR IF
•
•
•
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KEEP OUT OF REACH OF CHILDREN.
If swallowed, get medical help or contact a Poison Control Center
right away.
DIRECTIONS
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OTHER INFORMATION
temporarily relieves discomfort due to minor irritations of the eye or
exposure to wind and sun
lubricates to prevent further irritation or to relieve dryness of the
eye
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
you feel eye pain
changes in vision occur
redness or irritation of the eyes lasts
condition worsens or lasts more than 72 hours
put 1 or 2 drops in the affected eye(s) as needed
tightly snap on cap to seal
•
INACTIVE INGREDIENTS
benzalkonium chloride, boric acid, chlorobutanol, edetate disodium,
menthol, polysorbate 80, potassium
aspartate, purified water, pyridoxine hydrochloride, sodium borate
QUESTIONS OR COMMENTS?
1-877-636-2677 MON-FRI 9AM-5PM (EST)
PACKAGE/LABEL PRINCIPAL DISPLAY PANEL
ROHTO JOLT
hypromellose liquid
do not store above 25°C (77°F)
The Mentholatum Company
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:10 742-8 19 4
ROUTE OF ADMINISTRATION
OPHTHALMIC
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
HYPRO MELLO SE 2 9 0 6 ( 4 0 0 0 MPA.S) (UNII: 5EYA6 9 XGAT)
(HYPROMELLOSE 29 0 6
(40 0 0 MPA.S) - UNII:5EYA6 9 XGAT)
HYPROMELLOSE 29 0 6
(40 0 0 MPA.S)
3.5 mg
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
BENZALKO NIUM CHLO RIDE (UNII: F5UM2KM3W7)
BO RIC ACID (UNII: