Surf & Sand Resort Instant Hand Sanitizer

Surf and Sand Resort Instant Hand Sanitizer by

Drug Labeling and Warnings

Surf and Sand Resort Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by A.D.S. Sales Co. Inc., Ming Fai Innovative Skin Care Lab Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SURF AND SAND RESORT INSTANT HAND SANITIZER- alcohol gel 
A.D.S. Sales Co. Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Surf & Sand Resort Instant Hand Sanitizer

Drug Facts

Active Ingredient

Ethyl Alcohol 72% (v/v)

Purpose

Antibacterial

Uses

to help reduce bacteria on the skin.

Warnings

For external use only.   Flammable.

Keep away from fire or flame.

When using this product

Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop using 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 center immediately.

Directions

Squeeze a significan amount in your palm and rub hands until fully dry.

Rinse free.

Other information

Store below 110°F (43°C).

Inactive ingredients

Aqua (Water), Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Hydrolyzed jojoba Esters, Phenoxyethanol, Parfum(Fragrance), Aminomethyl Propanol, Tocopherol, Glycine Soja (Soybean) Oil, Aloe Barbadensis Leaf Juice, Citrus Aurantium Dulcis (Orange) Fruit Extract, Olea Europaea (Olive) Fruit Oil

Package Labeling:

SURF AND SAND RESORT INSTANT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79249-025
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.72 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
TOCOPHEROL (UNII: R0ZB2556P8)
SOYBEAN OIL (UNII: 241ATL177A)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ORANGE (UNII: 5EVU04N5QU)
OLIVE OIL (UNII: 6UYK2W1W1E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79249-025-00	25 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/15/2020	12/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/15/2020	12/31/2022

Labeler - A.D.S. Sales Co. Inc. (051216828)

Establishment
Name	Address	ID/FEI	Business Operations
Ming Fai Innovative Skin Care Lab Limited		663304471	manufacture(79249-025)

Revised: 3/2023

Document Id: f7ab7976-3756-950e-e053-6294a90a255a

34390-5

Set id: 684e740d-bafd-4f7d-9b7c-c773add8f5f5

Version: 3

Effective Time: 20230324