ALLANTOIN- advanced derma therapy spray 
Harmon Store 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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Harmon Advanced Derma Therapy Spray

Active ingredient

Allantoin 0.5%

Purpose

Skin Protectant

Uses

Temporarily protects and helps relieve chapped or cracked skin

Warnings

For external use only.

Contents under pressure. Do not puncture or incinerate. Do not store above 120 °F. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.

Do not use

  • on deep or puncture wounds
  • on animal bites
  • on serious burns

When using this product

  • avoid spraying in eyes

Stop use and ask a doctor if

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

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

​Directions

Other information

store at room temperature

Inactive ingredients

Water, Dimethyl Ether, Isostearyl Isostearate, Isopropyl Isostearate, PPG-3 Benzyl Ether Myristate, Pentaerythrityl Tetracaprylate/Caprate, Methylsilanol Hydroxyproline Aspartate, Glycerin, Butylene Glycol, Allium Cepa (Onion) Bulb Extract, Sucrose Palmitate, Glyceryl Stearate, Glyceryl Stearate Citrate, Sucrose, Mannan, Xanthan Gum, Cetyl Hydroxyethylcellulose, Rutin, Palmitoyl Tripeptide-1, Palmitoyl Tetrapeptide-7, Phaseolus Lunatus (Green Bean) SEed Extract, Phenoxyethanol, Fragrance, Potassium Sorbate, Salicylic Acid

Questions?

Call 1-866-964-0939

Principal Display Panel

Harmon FaceValues

Advanced Derma Therapy Spray

ALLANTOIN 0.5% - SKIN PROTECTANT

Dermatologist Tested

Paraben-Free

SHAKE WELL BEFORE USING.

NET WT 3 OZ (85 g)

Derma Therapy Spray - Harmon.jpg

ALLANTOIN 
advanced derma therapy spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63940-022
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN0.425 g  in 85 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
DIMETHYL ETHER (UNII: AM13FS69BX)  
ISOSTEARYL ISOSTEARATE (UNII: IV0Z586Z4Y)  
PPG-3 BENZYL ETHER MYRISTATE (UNII: 8075L58MKO)  
PENTAERYTHRITYL TETRACAPRYLATE/TETRACAPRATE (UNII: 832C4KF14X)  
GLYCERIN (UNII: PDC6A3C0OX)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
ONION (UNII: 492225Q21H)  
SUCROSE PALMITATE (UNII: 3OSQ643ZK5)  
GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)  
SUCROSE (UNII: C151H8M554)  
YEAST MANNAN (UNII: 91R887N59P)  
XANTHAN GUM (UNII: TTV12P4NEE)  
CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)  
RUTIN (UNII: 5G06TVY3R7)  
PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)  
PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)  
LIMA BEAN (UNII: 112YH1ZMX2)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SALICYLIC ACID (UNII: O414PZ4LPZ)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63940-022-0385 g in 1 CAN; Type 0: Not a Combination Product09/04/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34709/04/2015
Labeler - Harmon Store Inc. (804085293)

Revised: 11/2019
Document Id: 97df1dc8-3928-2fbf-e053-2a95a90a5d16
Set id: 343feda6-bf94-4ccf-bb3a-29f0cec42356
Version: 4
Effective Time: 20191121
 
Harmon Store Inc.