ANTI-BACTERIAL HAND VAMPIRE BLOOD- alcohol gel

Nazione: Stati Uniti

Lingua: inglese

Fonte: NLM (National Library of Medicine)

Principio attivo:

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

Commercializzato da:

Bath & Body Works, Inc.

Tipo di ricetta:

OTC DRUG

Indicazioni terapeutiche:

Antiseptic Decrease bacteria on hands.

Stato dell'autorizzazione:

OTC monograph not final

Scheda tecnica

ANTI-BACTERIAL HAND VAMPIRE BLOOD- ALCOHOL GEL
BATH & BODY WORKS, 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._
----------
DRUG FACTS
ACTIVE INGREDIENT
Alcohol 68%
PURPOSE
Antiseptic
USE
Decrease bacteria on hands.
WARNINGS
FOR EXTERNAL USE ONLY.
When using this product keep out of eyes. Stop use and ask a doctor if
irritation or redness develops.
FLAMMABLE
Keep away from flame or high heat.
KEEP OUT OF REACH OF CHILDREN
If swallowed, get medical help or contact a Poison Control Center
right away.
DIRECTIONS
Rub a dime sized drop into hands.
INACTIVE INGREDIENTS
Water (Aqua, Eau),
Isopropyl Alcohol, Fragrance (Parfum),
Carbomer, Propylene Glycol, Lactose,
Aminomethyl Propanol, Isopropyl Myristate, Aloe
Barbadensis Leaf Juice, Cellulose, Hydroxyethyl
Urea, Tocopheryl Acetate, Wheat Amino Acids,
Butyrospermum Parkii (Shea) Butter Extract,
Retinyl Palmitate, Hydroxypropyl
Methylcellulose, Ultramarines (CI 77007),
Red 33 (CI 17200), Red 40 (CI 16035), Yellow
5 (CI 19140), Ext. Violet 2 (CI 60730).
COMPANY INFORMATION
Bath & Body Works, Distr.
Reynoldsburg, Ohio 43068
1-800-395-1001
www.bathandbodyworks.com
PRODUCT PACKAGING
ANTI-BACTERIAL HAND VAMPIRE BLOOD
alcohol gel
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:6 26 70 -59 9 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 8 mL in 10 0 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:6 26 70 -59 9 5-
0
29 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct
12/14/20 20
0 6 /15/20 21
2
NDC:6 26 70 -59 9 5-
1
73 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct
12/14/20 20
0 6 /15/20 21
3
NDC:6 26 70 -59 9 5-
3
23