ORCHID BY H E B VANILLA BROWN SUGAR- ethyl alcohol liquid

Land: USA

Språk: engelsk

Kilde: NLM (National Library of Medicine)

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Last ned Preparatomtale (SPC)
03-03-2014

Aktiv ingrediens:

ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)

Tilgjengelig fra:

H E B

Administreringsrute:

TOPICAL

Resept typen:

OTC DRUG

Indikasjoner:

TO HELP REDUCE BACTERIA ON THE SKIN

Autorisasjon status:

OTC monograph not final

Preparatomtale

                                ORCHID BY H E B VANILLA BROWN SUGAR- ETHYL ALCOHOL LIQUID
H E B
_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._
----------
DRUG FACTS
ACTIVE INGREDIENT
ETHYL ALCOHOL 65%
PURPOSE
ANTISEPTIC
USES
TO HELP REDUCE BACTERIA ON THE SKIN
WARNINGS
FOR EXTERNAL USE ONLY. FLAMMABLE. KEEP AWAY FROM SOURCE OF HEAT OR
FIRE
WHEN USING THIS PRODUCT
AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER
STOP USING THIS PRODUCT AND ASK DOCTOR IF
IRRITATION OR REDNESS DEVELOPS AND LASTS
_KEEP OUT OF REACH OF CHILDREN_
IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON
CONTROL CENTER IMMEDIATELY
DIRECTIONS
APPLY SMALL AMOUNT TO YOUR PALM AND RUB HANDS TOGETHER BRISKLY UNTIL
DRY. CHILDREN UNDER 6 SHOULD BE SUPERVISED WHEN USING THIS PRODUCT
OTHER INFORMATION
STORE AT A TEMPERATURE BELOW 110°F (43°C)
QUESTIONS/COMMENTS?
1-866-695-3030
INACTIVE INGREDIENTS
WATER (AQUA), FRAGRANCE (PARFUM), PROPYLENE GLYCOL, CARBOMER,
GLYCERIN,
AMINOMETHYL PROPANOL, MANNITOL, CELLULOSE, HYDROXYPROPYL
METHYLCELLULOSE, ISOPROPYL MYRISTATE, TOCOPHERYL ACETATE, ALOE
BARBADENSIS LEAF JUICE, CAPRYLIC/CAPRIC TRIGLYCERIDE, CAMELLIA
SINENSIS
LEAF EXTRACT, VANILLA PLANIFOLIA FRUIT EXTRACT, IRON OXIDES (CI
77491), IRON
OXIDES (CI 77492), IRON OXIDES (CI 77499), YELLOW 5 (CI 19140), RED 33
(CI 17200), BLUE 1
(CI 42090)
LABEL COPY
ORCHID BY H E B VANILLA BROWN SUGAR
ethyl alcohol liquid
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:378 0 8 -40 5
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
ALCO HO L (UNII: 3K9 9 58 V9 0 M) (ALCOHOL - UNII:3K9 9 58 V9 0 M)
ALCOHOL
6 50 mg in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
PRO PYLENE GLYCO L (UNII: 6 DC9 Q16 7V3)
CARBO MER 9 3 4 (UNII: Z135WT9 20 8 )
GLYCERIN (UNII: PDC6 A3C0 OX)
AMINO METHYLPRO PANO L (UNII: L
                                
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