GUARD- ethyl alcohol gel

Guard by

Drug Labeling and Warnings

Guard by is a Otc medication manufactured, distributed, or labeled by Apollo Health and Beauty Care Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Ethyl Alcohol (80%)

Purpose

Antiseptic

Uses

For Personal hand hygiene to help the spread of bacteria and can be used in place of hand washing if soap and water are not available.

Warnings

• For External use only
• Flammable
• Keep away from source of heat or fire.

When using this product

Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Do not Inhale.

Do not use

• on children less than 2 months of age
• on open skin wounds
• on broken or damaged skin

Stop use and ask a doctor

If Irritation or redness develops and lasts.

Keep out of reach of children

In case of accidental ingestion, get medical help or contact a Poison Control Centre immediately

Directions

• For occasional and personal use
• Rub thoroughly into hands for at least 30 seconds. Allow to dry
• Children under 6 years should be supervised when using this product

Other Information

• Store at a temperature below 110 0F (43 0C)
• May discolor certain fabrics or surfaces

Inactive Ingredients

Water (Aqua), PEG-6, Fragrance (Parfum), Isopropyl Alcohol, Glycerin, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, AMP-Acrylates/Vinyl Isodecanate Crosspolymer

Questions or comments ?

1-866-695-3030

Principal Display Panel 2 oz

Principal Display Panel 8 oz

Principal Display Panel 15 oz

Principal Display Panel 32 oz

Principal Display Panel 40 oz

Principal Display Panel 64 oz

Principal Display Panel 128 oz

INGREDIENTS AND APPEARANCE

GUARD 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63148-626
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	800 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63148-626-10	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/23/2020
2	NDC: 63148-626-20	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/23/2020
3	NDC: 63148-626-30	443 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/23/2020
4	NDC: 63148-626-40	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/23/2020
5	NDC: 63148-626-50	1182 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/23/2020
6	NDC: 63148-626-60	1892 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/23/2020
7	NDC: 63148-626-70	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	11/23/2020

Labeler - Apollo Health and Beauty Care Inc (201901209)

Registrant - Apollo Health and Beauty Care Inc (201901209)

Establishment
Name	Address	ID/FEI	Business Operations
Apollo Health and Beauty Care Inc		201901209	manufacture(63148-626)