Velnue by Bodywell Natural Skin Care Inc VELNUE- ethanol liquid

Velnue by

Drug Labeling and Warnings

Velnue by is a Otc medication manufactured, distributed, or labeled by Bodywell Natural Skin Care Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Ethanol 70%

Purpose

Antiseptic.

Uses

• Hand Sanitizer to help reduce bacteria that potentially can cause disease. 
• For use when soap and water are not available.

Warnings

For external use only Flammable. Keep away from heat or flame.

Do not use in children less than 2 months of age.
on open skin or wounds.

When using this product keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

• if irritation occurs.
• These may be signs of a serious condition.

Keep out of reach of children.

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

Directions.

Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information.

Store between 15-30C (59-86F)
Avoid freezing & excessive heat above 40C(104F)

Inactive Ingredients.

Aqua, Bis-PEG-12 Dimethicone, Glycerin, PEG-7 Glyceryl Cocoate, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate (Vitamin E).

Product Image

INGREDIENTS AND APPEARANCE

VELNUE 
ethanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81441-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BIS-PEG-12 DIMETHICONE (70 MPA.S) (UNII: 2JDK5W22H4)
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81441-003-01	350 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/20/2021
2	NDC: 81441-003-02	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/20/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/20/2021

Labeler - Bodywell Natural Skin Care Inc (201162026)

Establishment
Name	Address	ID/FEI	Business Operations
Bodywell Natural Skin Care Inc		201162026	manufacture(81441-003)