Hand Sanitizer Cinnamon Apple Cider

Hand Sanitizer Cinnamon Apple Cider by

Drug Labeling and Warnings

Hand Sanitizer Cinnamon Apple Cider by is a Otc medication manufactured, distributed, or labeled by Base4 Ventures, LLC., Ganzhou Olivee Cosmetic Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZER CINNAMON APPLE CIDER- alcohol gel 
Base4 Ventures, LLC.

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Hand Sanitizer Cinnamon Apple Cider

Drug Facts

Active Ingredient

Alcohol Denat. 66% (V/V)

Purpose

Antiseptic

Uses

• hand sanitizer to help decrease bacteria on the skin.
• recommended for repeated use.

Warnings

• For external use only. 
• Flammable. 
• Keep away from heat or flame.
• Does not contain grain alcohol; do not drink. If taken internally will produce severe gastric disturbances.

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 redness or irritation develop and lasts.

Keep out of reach of children.

If swallowed, get medical help or contact a poison control center immediately.

Directions

• Rub dime sized amount between hands until dry.
• Supervise children in the use of this product. In the case of eye contact rinse eyes thoroughly with water

Other information

• Do not store above 105°F.
• May discolor some fabrics.

Inactive ingredients

Water, Acrylate/C10-30 Alkyl Acrylate Crosspolymer, Fragrance, Aminomethyl Propanol, FD&C Red No. 4, FD&C Yellow No. 5, FD&C Blue No. 1.

Package Labeling:

HAND SANITIZER CINNAMON APPLE CIDER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62651-053
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	66 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62651-053-01	29.5 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/08/2021	01/08/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/08/2021	01/08/2022

Labeler - Base4 Ventures, LLC. (137316126)

Establishment
Name	Address	ID/FEI	Business Operations
Ganzhou Olivee Cosmetic Co., Ltd.		543008195	manufacture(62651-053)

Revised: 10/2023

Document Id: 086c76d7-ec1b-6051-e063-6294a90a3695

34390-5

Set id: 04891c24-78e2-4587-a087-e25676969857

Version: 3

Effective Time: 20231023