DR. PALM HAND SANITIZER- alcohol denat gel

Dr. Palm Hand sanitizer by

Drug Labeling and Warnings

Dr. Palm Hand sanitizer by is a Otc medication manufactured, distributed, or labeled by SKINNYDIP LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Alcohol 75%

Purpose

Antiseptic

Uses

• Hand sanitizer to help reduce bacteria on the skin that could cause disease.
• For use when soap and water are not available

warnings

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

• Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Do not use 

• in children less than 2 months of age.
• on open skin wounds.

When using this product

• keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Directions

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

Keep out of reach of children.

•  If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Inactive Ingredients.

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Extract, Aminomethyl Propanol,Butylene Glycol, Glycerin, Water (Aqua).

Other information.

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

Product Image

INGREDIENTS AND APPEARANCE

DR. PALM HAND SANITIZER 
alcohol denat gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81236-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81236-001-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/20/2020
2	NDC: 81236-001-02	35 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/20/2020
3	NDC: 81236-001-03	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/20/2020
4	NDC: 81236-001-04	75 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/20/2020
5	NDC: 81236-001-05	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/20/2020
6	NDC: 81236-001-06	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/20/2020
7	NDC: 81236-001-07	465 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/20/2020
8	NDC: 81236-001-08	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/20/2020
9	NDC: 81236-001-09	975 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/20/2020
10	NDC: 81236-001-10	27 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/08/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/20/2020

Labeler - SKINNYDIP LIMITED (217094578)