SANSPRAY- antibacterial sanitizer spray spray

SANSPRAY by

Drug Labeling and Warnings

SANSPRAY by is a Otc medication manufactured, distributed, or labeled by Beacon Promotions Inc, Beacon Promotions Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug facts

Ethyl Alcohol (62%)

Ethyl Alcohol (62%)

Spray enough product on hands to cover
all surfaces. Rub hands together until dry.

Inactive ingredients

Deionized Water, Glycerin, Propylene Glycol, Tocopherol, Fragrance, Aloe Vera.

Purpose

Antiseptic

Purpose

Anticeptic

Directions

Spray enough product on hands to cover
all surfaces. Rub hands together until dry.

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.

Keep out of reach of children

Keep out of reach of children

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SANSPRAY 
antibacterial sanitizer spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70445-605
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE (UNII: V5VD430YW9)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70445-605-01	9.76 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2024
2	NDC: 70445-605-02	19.8 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2024
3	NDC: 70445-605-03	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2024
4	NDC: 70445-605-04	120 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	01/04/2024

Labeler - Beacon Promotions Inc (119056382)

Registrant - Beacon Promotions Inc. (119056382)

Establishment
Name	Address	ID/FEI	Business Operations
Beacon Promotions Inc.		119056382	manufacture(70445-605)