HAND GEL gel

Šalis: Jungtinės Valstijos

kalba: anglų

Šaltinis: NLM (National Library of Medicine)

Veiklioji medžiaga:

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

Prieinama:

Jean Pierre Inc.

Vartojimo būdas:

TOPICAL

Recepto tipas:

OTC DRUG

Terapinės indikacijos:

Antiseptic Hand sanitizer to help decrease bacteria on the skin when water, soap & towel are not available. Recommended for repeated use Do not apply around eyes. Do not use in ears or mouth. Stop use or ask for a doctor if redness or irritation develops and persists for more than 72 hours.

Autorizacija statusas:

OTC monograph not final

Prekės savybės

HAND GEL- HAND GEL GEL
JEAN PIERRE 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._
----------
70483-018
HAND GEL
ACTIVE INGREDIENT(S)
Ethyl Alcohol 70%
PURPOS E
Antiseptic
US E
Hand sanitizer to help decrease bacteria on the skin when water, soap
& towel are not available.
Recommended for repeated use
WARNINGS
DO NOT USE
Do not apply around eyes. Do not use in ears or mouth.
When using this product, avoid contact with eyes. In case of contact,
flush eyes with water.
Stop use or ask for a doctor if redness or irritation develops and
persists for more than 72 hours.
Keep out of reach of children. Children must be supervised in use of
this product.
Stop use or ask for a doctor if redness or irritation develops and
persists for more than 72 hours.
Keep out of reach of children. Children must be supervised in use of
this product.
DIRECTIONS
Squeeze as needed into your palms and thoroughly spread on bottom
hands. Rub into skin until dry.
OTHER INFORMATION
Do not store in temperature over 118°F.
INACTIVE INGREDIENTS
Water, Propylene Glycol, Glycerin, Carbomer, Aloe Barbadensis Leaf
Juice, Triethanolamine,
Fragrance. May Contain: FD & C Red No. 4, FD & C Blue No. 1, FD & C
Yellow No 5.
PACKAGE LABEL - PRINCIPAL DISPLAY PANEL
HAND GEL
hand gel gel
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:70 48 3-0 18
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
70 mL in 10 0 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
GLYCERIN (UNII: PDC6 A3C0 OX)
PRO PYLENE GLYCO L (UNII: 6 DC9 Q16 7V3)
WATER (UNII: 0 59 QF0 KO0 R)
TRO LAMINE (UNII: 9 O3K9 3S3TK)
FRAGRANCE CLEAN O RC0 6 0 0 3 2 7 (UNII: 329 LCV5BTF)
FD&C RED NO . 4 0 (UNII: WZB9 127XOA)
FD&C BLUE NO . 1 (UNII: H3R47K3TBD)
FD&C YELLO W NO . 5 (UNII: