FF SILICONE SPRY SANI PPK liquid

FF SILICONE SPRY SANI PPK by

Drug Labeling and Warnings

FF SILICONE SPRY SANI PPK by is a Otc medication manufactured, distributed, or labeled by ZHEJIANG JINGHUI COSMETICS SHARE CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

ETHYL ALCOHOL 70% v/v

Purpose

ANTISEPTIC

Use

• To decrease bacteria on the skin that could cause disease.
• When water, soap and towel are not available.
• Recommended for repeated use.

Warnings

For external use only. Flammable, Keep away from fire or flame.

Do not use

Do not use it near eye area. In case of contact, rinse eyes thoroughly with water.

WHEN USING

• Keep out of eyes, ears, or mouth.
• In case of eye contact, flush eyes thoroughly with water.
• Avoid contact with broken skin.
• Do not inhale or ingest.

STOP USE

Stop use and ask a doctor if
Redness of irritation develop.
Condition persists for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.
Children should be supervised by an aduit when using this product.
If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Spray product in your palm and rub hands together until dry.
• For children under 6, use only under adult supervision.
• Not recommended for infants.

Other information

• Do not store above 105℉.
• May discolor some fabrics.
• Harmful to wood finishes and plastics.

Inactive ingredients

Water (Aqua), Glycerin, Aminomethyl Propanol, Fragrance, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate (Vitamin E). May Contain: Blue 1 (CI 42090), Red 33 (CI 17200), Yellow 5 (CI 19140).

PRINCIPAL DISPLAY PANEL

40mL 73905-046-01

INGREDIENTS AND APPEARANCE

FF SILICONE SPRY SANI PPK 
ff silicone spry sani ppk liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73905-046
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
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
RED 33 (UNII: 9DBA0SBB0L)
BLUE 1 (UNII: H3R47K3TBD)
YELLOW 5 (UNII: I753WB2F1M)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
AMINOMETHYL PROPANOL (UNII: LU49E6626Q)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73905-046-01	40 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/27/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	11/27/2025

Labeler - ZHEJIANG JINGHUI COSMETICS SHARE CO.,LTD (529558167)

Establishment
Name	Address	ID/FEI	Business Operations
ZHEJIANG JINGHUI COSMETICS SHARE CO.,LTD		529558167	manufacture(73905-046)