CVS ICHTHAMMOLOINTMENT SALVE- ichthammol ointment

国家: 美国

语言: 英文

来源: NLM (National Library of Medicine)

有效成分:

ICHTHAMMOL (UNII: NQ14646378) (ICHTHAMMOL - UNII:NQ14646378)

可用日期:

CVS Health

给药途径:

TOPICAL

处方类型:

OTC DRUG

疗效迹象:

Drawing Salve

授权状态:

unapproved drug other

产品特点

CVS ICHTHAMMOLOINTMENT SALVE- ICHTHAMMOL OINTMENT
CVS HEALTH
_Disclaimer: This drug has not been found by FDA to be safe and
effective, and this_
_labeling has not been approved by FDA. For further information about
unapproved_
_drugs, click here._
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CVS LCHTHAMMOL OINTMENT DRAWING SALVE
Drawing Salve
_DRUG FACTS_
_ACTIVE INGREDIENT_
_PURPOSE_
lchthammol USP 10%
Drawing Salve
_USES_
for drawing or removing splinters, slivers, or similar items
_WARNINGS_
For external use only.
_DRUG FACTS_ (CONTINUED)
DO NOT USE in eyes
ASK A DOCTOR BEFORE USE IF you have deep puncture wounds or serious
burns
STOP USE AND ASK DOCTOR IF redness, irritation, swelling or pain
persists
KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or
contact a Poison
Control Center right away.
_DRUG FACTS_ (CONTINUED)
_DIRECTIONS_
Cleanse affected area. Apply on gauze bandage once or twice a day.
Repeat as
necessary. Do not rub or massage affected area.
_OTHER INFORMATION_
Store at room temperature.
_INACTIVE INGREDIENTS_
Bis-diglyceryl polyacyladipate-2, Petrolatum
_QUESTIONS OR COMMENTS?_
1-800-635-3696
PACKAGE LABEL - TUBE CARTON
CVS ICHTHAMMOLOINTMENT SALVE
ichthammol ointment
CVS Health
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:69842-790
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
ICHTHAMMOL (UNII: NQ14646378) (ICHTHAMMOL - UNII:NQ14646378)
ICHTHAMMOL
100 mg in 1 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
BIS-DIGLYCERYL POLYACYLADIPATE-2 (UNII: 6L246LAM9T)
PETROLATUM (UNII: 4T6H12BN9U)
PRODUCT CHARACTERISTICS
COLOR
brown (To dark brown paste)
SCORE
SHAPE
SIZE
FLAVOR
IMPRINT CODE
CONTAINS
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:69842-790-
01
1 in 1 CARTON
07/01/2020
1
28 g in 1 TUBE; Type 0: Not a Combination
Product
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITATION
MARKETING START
DATE
MARKETING END
DATE
unapproved drug
other
07/01/2020
LABELER -
C