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DR DEEP AQUA WRINKLECREAM

Dosage form: cream
Ingredients: ALLANTOIN 1mL in 100mL, ADENOSINE 0.04mL in 100mL
Labeler: MineralHouse Corporation
NDC Code: 76015-400

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.

Active Ingredients: Allantoin 0.1%, Adenosine 0.04%

Purpose: Skin Protectant

Uses - Apply over the face, under-ey area and the neck thoroughly

Warnings - For external use only

Do Not Use - On wounds or damaged skin

When using this product:
- do not use other than directed

Stop use - If allergic reaction or irritation occurs

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

Direction:
Adults over 18 years old
 Step1: Clean and dry the face or the body
 Step2: Apply a proper amount to the face, under-eye area and the neck

Storage - Keep in a dry and cool place

Inactive Ingredients:
Aqua, Cyclopentasiloxane, Aloe Ferox Leaf, Lecithin, Butylene Glycol, Cyclomethicone, Glycerin, Dimethicone, Cetyl Peg/ppg-10/1 Dimethicone, Citrus Granis (Grapefruit) Fruit Extract, Chamomilla Recutita (Matricaria) Flower/Leaf/Stem, Camellia Sinensis Leaf Extract, Magnolia Biondii Bark Extract, Salix Alba(Willow) Bark Water

DR DEEP AQUA WRINKLECREAM 
allantoin adenosine cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76015-400
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (ALLANTOIN) ALLANTOIN1 mL  in 100 mL
ADENOSINE (ADENOSINE) ADENOSINE0.04 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
CYCLOMETHICONE 5 
GLYCERIN 
ALOE FEROX LEAF 
EGG PHOSPHOLIPIDS 
BUTYLENE GLYCOL 
CYCLOMETHICONE 
DIMETHICONE 
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) 
PUMMELO 
MATRICARIA RECUTITA FLOWERING TOP 
GREEN TEA LEAF 
MAGNOLIA BIONDII BARK 
SALIX ALBA BARK VOLATILE OIL 
Packaging
#Item CodePackage Description
1NDC:76015-400-01100 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34701/01/2012
Labeler - MineralHouse Corporation (557802539)
Registrant - MineralHouse Corporation (557802539)
Establishment
NameAddressID/FEIOperations
MineralHouse Corporation557802539relabel, repack
Establishment
NameAddressID/FEIOperations
BoBo Cosmetics, Co689778744manufacture

Revised: 01/2012
Document Id: ed677e76-e9c4-4ae9-b274-b1abdc050afd
Set id: 992043eb-d0e4-4caf-bb41-ef26c3f6a088
Version: 1
Effective Time: 20120101
 
MineralHouse Corporation

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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