DAYLOGIC SKIN RELIEF MOISTURIZING- dimethicone lotion 
Rite Aid Corporation

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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Drug Facts

Active ingredient

Dimethicone 1.3%

Purpose

Skin Protectant

Uses

temporarily protects and helps relieve chapped or cracked skin, and helps protect from the drying effects of wind and cold.

Warnings

For external use only.

When using this product

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

Stop use and ask a doctor if

condition worsens, or if irritation or redness develops and lasts more than 7 days, or clears up and recurs within a few days.

Keep out of reach of children.

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

apply as needed.

Inactive ingredients

Water (Aqua), Glycerin, Distearyldimonium Chloride, Petrolatum, Isopropyl Palmitate, Avena Sativa (Oat) Kernel Flour, Cetyl Alcohol, Sodium Chloride, Cetyl Hydroxyethylcellulose, Benzyl Alcohol, Fragrance (Parfum), Chlorphenesin.

Questions or comments?

1-866-695-3030

Label Copy

Image of the label

DAYLOGIC SKIN RELIEF MOISTURIZING 
dimethicone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-3221
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE13 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)  
PETROLATUM (UNII: 4T6H12BN9U)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
OAT (UNII: Z6J799EAJK)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
CETYL HYDROXYETHYLCELLULOSE (550000 MW) (UNII: 2MIM45ZIL3)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11822-3221-8532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/08/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34702/08/2018
Labeler - Rite Aid Corporation (014578892)
Registrant - Apollo Health and Beauty Care Inc. (201901209)
Establishment
NameAddressID/FEIBusiness Operations
Apollo Health and Beauty Care Inc.201901209manufacture(11822-3221)

Revised: 2/2018
Document Id: 4e20fadc-8265-4df6-9774-a4e1f072910a
Set id: 5dee926f-1e29-4d0b-bd56-0ebbf50115c8
Version: 1
Effective Time: 20180209
 
Rite Aid Corporation