PHARMACY PRESCRIPTION 1.8OZ HAND SANITIZER - SWEET PEACH- alcohol gel

Nchi: Marekani

Lugha: Kiingereza

Chanzo: NLM (National Library of Medicine)

Viambatanisho vya kazi:

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

Inapatikana kutoka:

Ningbo Liyuan Daily Chemical Products Co.,Ltd.

Njia ya uendeshaji:

TOPICAL

Dawa ya aina:

OTC DRUG

Matibabu dalili:

Antimicrobial - Helps reduce bacteria on the skin that could cause disease. Recommended for repeated use. irritation and redness develops and lasts more than 72 hours.

Idhini hali ya:

OTC monograph not final

Tabia za bidhaa

PHARMACY PRESCRIPTION 1.8OZ HAND SANITIZER - SWEET PEACH- ALCOHOL GEL
NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO.,LTD.
_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._
----------
ACTIVE INGREDIENT
Ethyl Alcohol 62.0%
PURPOS E
Antimicrobial
US ES
- Helps reduce bacteria on the skin that could cause disease.
Recommended for repeated use.
WARNINGS
FOR EXTERNAL USE ONLY.
FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME.
WHEN USING THIS PRODUCT
do not use in or near the eyes. In case of eye contact, flush eyes
thoroughly with water.
STOP USE AND ASK A DOCTOR IF:
irritation and redness develops and lasts more than 72 hours.
KEEP OUT OF REACH OF CHILDREN.
If swallowed, get medical help or contact a Poison Control Center
right away.
DIRECTIONS -
Place enough product in palm to thoroughly cover your hands. Rub hands
together briskly until dry.
Children under 6 years of age should be supervised when using this
product.
Other information: Store below 110 Fahrenheit degree (43 degrees
Celsius)
May discolor certain fabrics or surfaces.
INACTIVE INGREDIENTS:
Water, Aloe Barbadensis Gel, Carbomer, Fragrance, Glycerin,
Triethanolamine, Tocopheryl Acetate,
(Sweet Peach FD&C Red No. 40, FD&C Yellow No. 5)
DRUG FACTS
PHARMACY PRESCRIPTION 1.8OZ HAND SANITIZER - SWEET PEACH
alcohol gel
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:76 176 -0 72
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 2 mL in 10 0 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
Ningbo Liyuan Daily Chemical Products Co.,Ltd.
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:76 176 -0 72-
0 1
53 mL in 1 BOTTLE, PLASTIC; Type 0 : No t a Co mbinatio n
Pro duc t
0 1/0 1/20 18
MARKETING I