SHINGLES PAIN RELIEF CREAM- roycederm shingles pain relief cream cream

देश: संयुक्त राज्य

भाषा: अंग्रेज़ी

स्रोत: NLM (National Library of Medicine)

सक्रिय संघटक:

WORMWOOD (UNII: F84709P2XV) (WORMWOOD - UNII:F84709P2XV)

थमां उपलब्ध:

Ehy Holdings LLC

प्रशासन का मार्ग:

TOPICAL

प्रिस्क्रिप्शन प्रकार:

OTC DRUG

चिकित्सीय संकेत:

for shingles skin care For the treatment of symptomsof shingles, hives, and rashes. it on pregnant womenand children under 12 years ofage unless directed by a doctor condition worsens or does notimprove after regular use asdirected

प्राधिकरण का दर्जा:

unapproved drug other

उत्पाद विशेषताएं

SHINGLES PAIN RELIEF CREAM- ROYCEDERM SHINGLES PAIN RELIEF CREAM CREAM
EHY HOLDINGS LLC
_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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81799-009
SHINGLES PAIN RELIEF CREAM
ACTIVE INGREDIENT(S)
Artemisia extract [fhfi] 3%
PURPOSE
for shingles skin care
USE
For the treatment of symptomsof shingles, hives, and rashes.
WARNINGS
FOR EXTERNAL USE ONLY
DO NOT USE
it on pregnant womenand children under 12 years ofage unless directed
by a doctor
avoid contact with eyeslf contact occurs, rinse the eyesthoroughly
with water.
condition worsens or does notimprove after regular use asdirected
If swallowed, getmedical help or contact aPoison Control
Center(1-800-222-1222) right
away.
DIRECTIONS
Apply a small amount to theproblem areas with circularmotions for 3
minutes till theskin
absorbs the cream.
Apply it 2-3 times a day for thebest result.
OTHER INFORMATION
Store at room temperature andout of direct sunlight
INACTIVE INGREDIENTS
Water, Sophora Flavescens Root,Cnidium Monnieri Fruit, KochiaScoparia
Pollen,
Dictamnus Dasyca-rpus Root, Smilax Glabra Whole
if you are allergic to ingredientsin this product.
Visit www.roycederm.com
PACKAGE LABEL - PRINCIPAL DISPLAY PANEL
81799-009-01
SHINGLES PAIN RELIEF CREAM
roycederm shingles pain relief cream cream
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:81799-009
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
WORMWOOD (UNII: F84709P2XV) (WORMWOOD - UNII:F84709P2XV)
WORMWOOD
3 g in 100 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
Ehy Holdings LLC
DICTAMNUS DASYCARPUS ROOT (UNII: 6153LEN214)
WATER (UNII: 059QF0KO0R)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
SMILAX GLABRA WHOLE (UNII: H51N91QNEB)
CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS)
BASSIA SCOPARIA POLLEN (UNII: 07A108ZKW5)
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING