SANSPRAY-NA- non-alcohol antibacterial hand sanitizer spray

Negara: Amerika Serikat

Bahasa: Inggris

Sumber: NLM (National Library of Medicine)

Bahan aktif:

BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)

Tersedia dari:

Beacon Promotions, Inc.

Rute administrasi :

TOPICAL

Jenis Resep:

OTC DRUG

Indikasi Terapi:

Antiseptic Anticeptic

Karakteristik produk

SANSPRAY-NA- NON-ALCOHOL ANTIBACTERIAL HAND SANITIZER SPRAY
BEACON PROMOTIONS, INC.
----------
HAND SANITIZER SPRAY
PURPOSE
Antiseptic
WARNINGS:
For external use only. Flammable. Keep away from heat or flame. Keep
out of eyes, ears
& mouth. In case of contact with eyes, rinse eyes thoroughly with
water. Stop use and
ask doctor if
redness or irritation develop and persist for more than 72 hours. Keep
out of reach of
children.
If swallowed, get medical help or contact a Poison Control Center
right away.
Do not use on children less than 2 months of age. Do not use on open
skin wounds.
DIRECTIONS
Spray enough product on hands to cover
all surfaces. Rub hands together until dry.
INACTIVE INGREDIENT:
Water, Aloe Vera, Glycerin, Propylene Glycol, Tocopherol, Lemon
Fragrance.
PURPOSE
Anticeptic
DRUG FACTS
Active Ingredient Purpose
Benzalkonium Chloride (0.1%)
Spray enough product on hands to cover
all surfaces. Rub hands together until dry.
KEEP OUT OF REACH OF CHILDREN
keep out of reach of children
SANSPRAY-NA
non-alcohol antibacterial hand sanitizer spray
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:70445-606
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
UNII:7N6JUD5X6Y)
BENZ ALKONIUM
CHLORIDE
1 mg
in 100 mL
Beacon Promotions, Inc.
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE (UNII: V5VD430YW9)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:70445-
606-01
9.76 mL in 1 BOTTLE, SPRAY; Type 0: Not a
Combination Product
01/03/2024
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITATION
MARKETING START
DATE
MARKETING END
DATE
OTC Monograph Drug
M003
01/03/2024
LABELER -
Beacon Promotions, Inc. (119056382)
ESTABLISHMENT
NAME
ADDRESS
ID/FEI
BUSINESS OPERATIONS
Beacon Promotions Inc