Label: DT COLLAGEN- octocrylene cream
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Contains inactivated NDC Code(s)
NDC Code(s): 70522-001-01 - Packager: DT Collagen, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated December 15, 2017
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
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INACTIVE INGREDIENT
Aqua, vinyl dimethicone copolymer, shea butter, C13-14 isoparafin, caprylic/capric triglyceride, ceramide2, cetearyl alcohol, cetyl alcohol, cyclomethicone, dimethicone, di=panthenol, ethylhexyl palimitate, ethylhexylglycerin, glycerin, glyceryl stearate, hyaluronic acid, laureth-7, PEG-100, stearate, phenoxyethanol, polyacrylamide, polosorbate 20, propyleneylycol, soluble collagen, tocopheryl acetate, triethanolamine
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INGREDIENTS AND APPEARANCE
DT COLLAGEN
octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70522-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 10 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 10 mg in 1 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SHEA BUTTER (UNII: K49155WL9Y) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETYL ALCOHOL (UNII: 936JST6JCN) DIMETHICONE 100 (UNII: RO266O364U) PANTHENOL (UNII: WV9CM0O67Z) ETHYLHEXYL PALMITATE (UNII: 2865993309) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) HYALURONIC ACID (UNII: S270N0TRQY) LAURETH-7 (UNII: Z95S6G8201) PEG-100 STEARATE (UNII: YD01N1999R) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I) POLYSORBATE 20 (UNII: 7T1F30V5YH) COLLAGEN, SOLUBLE, FISH SKIN (UNII: 8JC99XGU4W) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) .ALPHA.-TOCOTRIENOL (UNII: B6LXL1832Y) TRIETHANOLAMINE OLEATE (UNII: DZ7P3IE35F) CAPRYLIC/CAPRIC/LINOLEIC TRIGLYCERIDE (UNII: U73D397055) CERAMIDE 2 (UNII: C04977SRJ5) CYCLOMETHICONE (UNII: NMQ347994Z) PROPYLENE GLYCOL 2-OLEATE (UNII: R3FST8K0ZL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70522-001-01 50 mL in 1 TUBE; Type 0: Not a Combination Product 01/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 01/01/2016 Labeler - DT Collagen, Inc. (011478279) Registrant - DT Collagen (011478279) Establishment Name Address ID/FEI Business Operations Pure Source 080354456 manufacture(70522-001)