Label: TIEGE HANLEY AM MORNING FACIAL MOISTURIZER WITH SPF 20- avobenzene, octinoxate, octocrylene lotion
- NDC Code(s): 71714-001-22, 71714-001-75
- Packager: TIEGE HANLEY, Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated September 13, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- WARNINGS
-
DOSAGE & ADMINISTRATION
Directions
■ After washing your face, massage a pea-sized
amount into entire face and neck in a gentle circular motion
■ Before sun exposure, use a broad-spectrum sunscreen of SPF
15 or higher
■ Reapply sunscreen at least every two hours
■ Use a water-resistant sunscreen if swimming or sweating
■ For children under 6 months, ask a doctor - INDICATIONS & USAGE
-
INACTIVE INGREDIENT
Water
Isodecyl Neopentanoate
Cyclopentasiloxane
Bis-PEG-12 Dimethicone Beeswax
Glycerin
Glyceryl Stearate
PEG-100 Stearate
Phenoxyethanol
Hydroxypropyl Starch Phosphate
C18-38 Alkyl Hydroxystearoyl Stearate
Caprylyl Glycol
Carbomer
Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer
Isohexadecane
Lavandula Angustifolia (Lavender) Oil
Rosmarinus Officinalis (Rosemary) Leaf Oil
Sodium Hydroxide
Polysorbate 80
Calendula Officinalis Flower Extract
Plantago Major Leaf Extract
Disodium EDTA
- Tiege Hanley AM Morning Facial Moisturizer with SPF 20 - 0.75 FL. OZ. / 22mL
- Tiege Hanley AM Morning Facial Moisturizer with SPF 20 - 2.5 FL. OZ. / 75mL
-
INGREDIENTS AND APPEARANCE
TIEGE HANLEY AM MORNING FACIAL MOISTURIZER WITH SPF 20
avobenzene, octinoxate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71714-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 25 mg in 1 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 55 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) BIS-PEG-12 DIMETHICONE (70 MPA.S) (UNII: 2JDK5W22H4) GLYCERIN (UNII: PDC6A3C0OX) SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX) PLANTAGO MAJOR LEAF (UNII: 7DC28K241X) LAVENDER OIL (UNII: ZBP1YXW0H8) ISODECYL NEOPENTANOATE (UNII: W60VYE24XC) HYDROXYPROPYL CORN STARCH (5% SUBSTITUTION BY WEIGHT) (UNII: 9M44R3409A) CARBOMER 940 (UNII: 4Q93RCW27E) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SODIUM HYDROXIDE (UNII: 55X04QC32I) POLYSORBATE 80 (UNII: 6OZP39ZG8H) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) TETRADECYLOCTADECYL STEARATE (UNII: VX3T5G31XA) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) ISOHEXADECANE (UNII: 918X1OUF1E) ROSEMARY OIL (UNII: 8LGU7VM393) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71714-001-22 22 mL in 1 TUBE; Type 0: Not a Combination Product 09/30/2017 2 NDC:71714-001-75 75 mL in 1 TUBE; Type 0: Not a Combination Product 09/30/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 09/30/2017 Labeler - TIEGE HANLEY, Inc (080305325)