PALMA HAND SANITIZER- ethyl alcohol gel

PALMA HAND SANITIZER by

Drug Labeling and Warnings

PALMA HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by UNITRADE FZE. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl alcohol 70% v/v

Purpose

Antiseptic

Uses 

hand sanitizer to decrease bacteria on the skin  recommended for repeated use  for use when soap and water are not available

Warnings

Flammable, keep away from fire/flame
For external use only

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

When using this product do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if  irritation and redness develop  condition persists for more than 72 hours

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

wet hands thoroughly with product and allow to dry without wiping supervise children under 6 years of age when using this product to avoid swallowing

Other information

store between 15-30°C (59-86°F) avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

water, caprylic /capric triglyceride, avocado (Persea gratissima) oil, propylene glycol, glycerin, jojoba (Simmondsia chinensis) seed oil, peg-40 hydrogenated castor oil, polyacrylamide, c13-14 isoparaffin, laureth-7, acrylates / c10-30 alkyl acrylates crosspolymer, niacinamide, sodium hyaluronate, tocopheryl acetate, panthenol, gotu kola (Centella asiatica) root extract, triethanolamine, fragrance.

Questions? 1-516-535-5555

You may also report serious side effects to this phone number. Mon-Fri 9:00 AM - 5:00 PM

SPL UNCLASSIFIED SECTION

MOISTURIZING

WITH AVOCADO OIL, JOJOBA OIL, VITAMIN B3 & B5

PROTECT. HYDRATE. NOURISH.

Distributed by:
Palma De Salus, Inc
320 Country Road, Suite 205
Garden City, NY 11530, U.S.A

Made in U.A.E.
Designed in Los Angeles
palmadesalus.com

Packaging

INGREDIENTS AND APPEARANCE

PALMA HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81286-101
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)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
AVOCADO OIL (UNII: 6VNO72PFC1)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
JOJOBA OIL (UNII: 724GKU717M)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
POLYACRYLAMIDE (1300000 MW) (UNII: SC5Y4X78TG)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
LAURETH-7 (UNII: Z95S6G8201)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
NIACINAMIDE (UNII: 25X51I8RD4)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PANTHENOL (UNII: WV9CM0O67Z)
CENTELLA ASIATICA LEAF (UNII: 6810070TYD)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81286-101-10	1 in 1 CARTON	07/26/2021
1		325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/26/2021

Labeler - UNITRADE FZE (864268417)