SULPHUR- sulfur tablet

Riik: Ameerika Ühendriigid

keel: inglise

Allikas: NLM (National Library of Medicine)

Toimeaine:

SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)

Saadav alates:

Hyland's

Manustamisviis:

ORAL

Retsepti tüüp:

OTC DRUG

Näidustused:

Homeopathic Medicine RASHES & ECZEMA

Volitamisolek:

unapproved homeopathic

Toote omadused

SULPHUR- SULFUR TABLET
HYLAND'S
_Disclaimer: This homeopathic product has not been evaluated by the
Food and Drug Administration for_
_safety or efficacy. FDA is not aware of scientific evidence to
support homeopathy as effective._
----------
SULPHUR 6X
SULPHUR 6X
HOMEOPATHIC MEDICINE
RASHES & ECZEMA
MADE ACCORDING TO THE HOMEOPATHIC PHARMACOPOEIA OF THE UNITED STATES
SINCE 1903.
WARNINGS
Do not use if cap band is missing or broken.
If you are pregnant or nursing, consult a licensed health care
professional before using this product.
If symptoms persist for 7 days or worsen, contact a licensed
practitioner.
Keep this and all medicines out of the reach of children.
To be used according to label indications and/or standard homeopathic
indications.
DIRECTIONS
ADULTS: DISSOLVE 4 TABLETS UNDER TONGUE 4 TIMES A DAY.
CHILDREN: CONSULT A HEALTHCARE PROFESSIONAL.
INACTIVE INGREDIENTS
ACACIA GUM AND LACTOSE
QUES TIONS ?
800-624-9659
PRINCIPAL DISPLAY PANEL - 250 TABLET BOTTLE LABEL
SINCE 1903
HYLAND'S
HOMEOPATHIC
NDC 54973-0627-4
SULPHUR
6X
RASHES & ECZEMA*
250 TABLETS
*CLAIMS ARE BASED ON TRADITIONAL
®
HOMEOPATHIC PRACTICE, NOT ACCEPTED
MEDICAL EVIDENCE.
NOT FDA EVALUATED.
SULPHUR
sulfur tablet
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:549 73-0 6 27
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
SULFUR (UNII: 70 FD1KFU70 ) (SULFUR - UNII:70 FD1KFU70 )
SULFUR
6 [hp_X]
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
ACACIA (UNII: 5C540 3N26 O)
LACTO SE (UNII: J2B2A4N9 8 G)
Hyland's
PRODUCT CHARACTERISTICS
COLOR
ye llo w
S CORE
no sco re
S HAP E
ROUND
S IZ E
9 mm
FLAVOR
IMPRINT CODE
CONTAINS
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:549 73-0 6 27-
4
250 in 1 BOTTLE, PLASTIC; Type 0 : No t a Co mbinatio n
Pro duc t
0 1/0 1/19 55
MARKETING INFORMATION
MARKE TING CATE GORY
APPLICATION NUMBE R OR MONOGRAPH CITATION
MARKE TING START DATE
MARKE TING END DATE
unappro ved ho meo pathic
0 1/0 1/19