SANMO-WH- antibacterial hand sanitizer with white beads gel SANMO-RD- hand sanitizer with red beads gel SANMO-BL- antibacterial hand sanitizer with blue beads gel SANMO-GR- antibacterial hand sanitizer with green beads gel SAN-UN- antibacterial hand sanitizer unscented gel

SAN-UN by

Drug Labeling and Warnings

SAN-UN 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%

Put enough product in your palm to cover your hands and rub together
briskly until dry

Purpose

Antimicrobial

USE

Hand sanitizer to help decrease bacteria on the skin

Warnings

Flammable. Keep away from fire or flame.

■ For external use only.

■ When using this product do not
use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

■ Stop use and
ask a doctor if irritation or rash appears and lasts.

■ Keep out of reach of children.

If swallowed,get medical help or contact a Poison Control Center right away

Keep out of reach of children

Keep out of reach of children

Directions

■ Put enough product in your palm to cover your hands and rub together
briskly until dry

■ Children under 6 years of age should be supervised when using this
product

Drug Facts

Ethyl alcohol 62% v/v

Inactive Ingredients

Water, Polyethylene Glycol, Propylene Glycol, Vinyl Isodecanoate
Crosspolymer, Lactose, Cellulose, Tocopheryl Acetate, Aloe Barbadensis Leaf Extract,
Kaolin, Ultramarines, Hydroxypropyl Methylcellulose, Retinyl Palmitate, Fragrance

Other

■ Store at room temperature

■ May discolor certain fabrics or surfaces

SANMO Blue Beads

SANMO Red Beads

SANMO Green Beads

SANMO - Unscented

SANMO White Beads

INGREDIENTS AND APPEARANCE

SANMO-WH 
antibacterial hand sanitizer with white beads gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70445-601
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	63 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)
ALOE (UNII: V5VD430YW9)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MICROCRYSTALLINE CELLULOSE 101 (UNII: 7T9FYH5QMK)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70445-601-01	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
2	NDC: 70445-601-02	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
3	NDC: 70445-601-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
4	NDC: 70445-601-04	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
5	NDC: 70445-601-05	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
6	NDC: 70445-601-06	240 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/03/2024
7	NDC: 70445-601-07	300 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/03/2024
8	NDC: 70445-601-08	480 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
9	NDC: 70445-601-09	480 mL in 1 BOTTLE, PUMP; 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

SANMO-RD 
hand sanitizer with red beads gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70445-600
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
WATER (UNII: 059QF0KO0R)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
FERRIC OXIDE RED (UNII: 1K09F3G675)
ALOE (UNII: V5VD430YW9)
POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MICROCRYSTALLINE CELLULOSE 101 (UNII: 7T9FYH5QMK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70445-600-01	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2024
2	NDC: 70445-600-02	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2024
3	NDC: 70445-600-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2024
4	NDC: 70445-600-04	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2024
5	NDC: 70445-600-05	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2024
6	NDC: 70445-600-06	240 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/01/2024
7	NDC: 70445-600-07	300 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/01/2024
8	NDC: 70445-600-08	480 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2024
9	NDC: 70445-600-09	480 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/01/2024

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

SANMO-BL 
antibacterial hand sanitizer with blue beads gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70445-602
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	63 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
MICROCRYSTALLINE CELLULOSE 101 (UNII: 7T9FYH5QMK)
WATER (UNII: 059QF0KO0R)
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
KAOLIN (UNII: 24H4NWX5CO)
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
ALOE (UNII: V5VD430YW9)
ULTRAMARINE BLUE (UNII: I39WR998BI)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70445-602-01	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
2	NDC: 70445-602-02	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
3	NDC: 70445-602-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
4	NDC: 70445-602-04	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
5	NDC: 70445-602-05	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
6	NDC: 70445-602-06	240 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/03/2024
7	NDC: 70445-602-07	300 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/03/2024
8	NDC: 70445-602-08	480 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
9	NDC: 70445-602-09	480 mL in 1 BOTTLE, PUMP; 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

SANMO-GR 
antibacterial hand sanitizer with green beads gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70445-603
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
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE (UNII: V5VD430YW9)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
WATER (UNII: 059QF0KO0R)
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)
MICROCRYSTALLINE CELLULOSE 101 (UNII: 7T9FYH5QMK)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
CHROMIUM HYDROXIDE GREEN (UNII: RV8FT8XF5R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70445-603-01	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
2	NDC: 70445-603-02	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
3	NDC: 70445-603-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
4	NDC: 70445-603-04	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
5	NDC: 70445-603-05	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
6	NDC: 70445-603-06	240 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/03/2024
7	NDC: 70445-603-07	300 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/03/2024
8	NDC: 70445-603-08	480 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
9	NDC: 70445-603-09	480 mL in 1 BOTTLE, PUMP; 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

SAN-UN 
antibacterial hand sanitizer unscented gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70445-604
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	63 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE (UNII: V5VD430YW9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70445-604-01	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
2	NDC: 70445-604-02	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
3	NDC: 70445-604-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
4	NDC: 70445-604-04	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
5	NDC: 70445-604-05	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
6	NDC: 70445-604-06	240 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/03/2024
7	NDC: 70445-604-07	300 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/03/2024
8	NDC: 70445-604-08	480 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2024
9	NDC: 70445-604-09	480 mL in 1 BOTTLE, PUMP; 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.		119056382	manufacture(70445-601, 70445-602, 70445-603, 70445-604, 70445-600)