HUMCO STRONG IODINE TINCTURE- iodine tincture liquid

Land: Verenigde Staten

Taal: Engels

Bron: NLM (National Library of Medicine)

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Download Productkenmerken (SPC)
21-06-2020

Werkstoffen:

Iodine 7%, Potassium Iodide 5%, alcohl 85%

Beschikbaar vanaf:

Humo Holding Group, Inc.

Toedieningsweg:

TOPICAL

Prescription-type:

OTC DRUG

therapeutische indicaties:

Antiseptic To prevent infection in mior cuts, scrapes, and burns. The condition persists or gets worse, or if using for longer than once a week.

Autorisatie-status:

OTC monograph not final

Productkenmerken

                                HUMCO STRONG IODINE TINCTURE- IODINE TINCTURE LIQUID
HUMO HOLDING GROUP, INC.
_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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HUMCO STRONG IODINE TINCTURE
Drug Facts
ACTIVE INGREDIENTS
Iodine 7%
Potassium Iodide 5%
alcohl 85%
PURPOS E
Antiseptic
US ES
To prevent infection in mior cuts, scrapes, and burns.
WARNINGS
For external use only
ASK A DOCTOR IF YOU HAVE:
deep or puncture wounds
animal bites
serious burns.
STOP USE AND CONSULT A DOCTOR IF:
The condition persists or gets worse, or if using for longer than once
a week.
WHEN USING THIS PRODUCT:
Do not use in the eyes. If contact occurs, flush with large amounts of
water lifting upper and lower lids.
do not apply over large areas of the body.
KEEP OUT OF REACH OF CHILDREN
In case of accidental ingestion, give milk then a starch solution made
by mixing two tablespoonfuls of
cornstarch or flour to a pint of water. contact a Poison Control
Center immediately.
DIRECTIONS
Clean affacted area
Apply a small amount on the area 1 to 3 times daily.
May be covered with sterile bandage.
If bandaged, let it dry first.
INACTIVE INGREDIENT
Purified water
PRINCIPAL DISPLAY PANEL
Label
HUMCO STRONG IODINE TINCTURE
iodine tincture liquid
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:0 39 5-1219
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
IO DINE (UNII: 9 6 79 TC0 7X4) (IODINE - UNII:9 6 79 TC0 7X4)
IODINE
70 mg in 1 mL
PO TASSIUM IO DIDE (UNII: 1C4QK22F9 J) (IODIDE ION - UNII:0 9 G4I6 V8
6 Q)
IODIDE ION
50 mg in 1 mL
ALCO HO L (UNII: 3K9 9 58 V9 0 M) (ALCOHOL - UNII:3K9 9 58 V9 0 M)
ALCOHOL
8 50 mg in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:0 39 5-1219 -
16
473 mL in 1 BOTTLE, PLASTIC; Type 
                                
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