SANSPRAY-NA- non-alcohol antibacterial hand sanitizer spray

Country: মার্কিন যুক্তরাষ্ট্র

ভাষা: ইংরেজি

সূত্র: NLM (National Library of Medicine)

সক্রিয় উপাদান:

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

থেকে পাওয়া:

Beacon Promotions, Inc.

প্রশাসন রুট:

TOPICAL

প্রেসক্রিপশন টাইপ:

OTC DRUG

থেরাপিউটিক ইঙ্গিত:

Antiseptic Anticeptic

পণ্য বৈশিষ্ট্য

SANSPRAY-NA- NON-ALCOHOL ANTIBACTERIAL HAND SANITIZER SPRAY
BEACON PROMOTIONS, INC.
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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