BODEWELL ECZEMA DAILY SOOTHING- colloidal oatmeal spray 
The Procter & Gamble Manufacturing Company

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Bodewell Eczema Daily Soothing Spray

Drug Facts

Active ingredients

Colloidal Oatmeal 1%

Purpose

Skin Protectant

Uses

  • Temporarily protects and helps relieve minor skin irritation and itching due to: eczema rashes

Warnings

For external use only

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

Do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

Don't spray directly into your face.

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

Directions

Apply as needed

Water, glycerin, niacinamide, phenoxyethanol, 1,2-hexanediol, caprylyl glycol, aminomethyl propanol, sodium citrate, acrylates/C10-30 alkyl acrylate crosspolymer, polysorbate 20, citric acid, alcohol, hamamelis virginiana (witch hazel) bark/leaf extract, avena sativa (oat)
seed extract, populus alba bark extract, populus tremuloides bark extract, cochlearia officinalis flower/leaf/stalk extract, phytolacca decandra root extract, lens esculenta (lentil) fruit extract, berberis vulgaris bark extract, scrophularia nodosa extract, veronica officinalis extract, sanguinaria canadensis rhizome/root extract, althaea officinalis root extract, chamomilla recutita (matricaria) flower extract, sambucus nigra extract, achillea millefolium extract, aesculus hippocastanum (horse chestnut) seed extract, malva sylvestris (mallow) leaf extract, nasturtium officinale leaf extract, smilax medica root extract, tussilago farfara (coltsfoot) leaf extract, pimpinella saxifraga extract, vincetoxicum hirundinaria root extract

Questions (or comments)?

1-800-213-1873

Dist. by The Procter & Gamble Distributing, LLC

Cincinnati, OH 45202

MADE IN USA of U.S. and/or Importing Ingredients

bodewellskin.com

PRINCIPAL DISPLAY PANEL - 118 mL Bottle

Bodewell

eczema daily

soothing spray

Colloidal Oatmeal

Skin Protectant

4.0 FL OZ (118 mL)

Bodewell

BODEWELL ECZEMA DAILY SOOTHING 
colloidal oatmeal spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-615
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y) OATMEAL1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
MALVA SYLVESTRIS LEAF (UNII: 17H39B00T5)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
SMILAX ARISTOLOCHIAEFOLIA ROOT (UNII: NR100Y25G0)  
TUSSILAGO FARFARA LEAF (UNII: G2GH7V846Z)  
NIACINAMIDE (UNII: 25X51I8RD4)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
LENS CULINARIS FRUIT (UNII: ZYZ076G9JH)  
ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H)  
PIMPINELLA SAXIFRAGA WHOLE (UNII: LCL1491142)  
CHAMOMILE (UNII: FGL3685T2X)  
COCHLEARIA OFFICINALIS FLOWERING TOP (UNII: M87UN67CKR)  
NASTURTIUM OFFICINALE LEAF (UNII: 362629QKRT)  
PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)  
POPULUS ALBA BARK (UNII: K12723D3GV)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
SAMBUCUS NIGRA WHOLE (UNII: 4X6JT95SYN)  
SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)  
HORSE CHESTNUT (UNII: 3C18L6RJAZ)  
VINCETOXICUM HIRUNDINARIA ROOT (UNII: 9R858U917W)  
HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)  
SCROPHULARIA NODOSA (UNII: 7H443NUB2T)  
BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)  
ACHILLEA MILLEFOLIUM WHOLE (UNII: 2FXJ6SW4PK)  
ALCOHOL (UNII: 3K9958V90M)  
POPULUS TREMULOIDES BARK (UNII: 5543O0CEID)  
VERONICA OFFICINALIS WHOLE (UNII: 9EHR580PSP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69423-615-11118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product02/15/202204/30/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01602/15/202204/30/2024
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 11/2023
Document Id: 0a33fa8a-8af2-30ed-e063-6394a90a1808
Set id: d928bd2c-c00b-38d0-e053-2a95a90ad02c
Version: 2
Effective Time: 20231115
 
The Procter & Gamble Manufacturing Company