Label: 12 DAYS OF DERM-LOVED SKINCARE- octinoxate, zinc oxide, oatmeal, benzoyl peroxide, avobenzone, octisalate, octocrylene kit
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NDC Code(s):
14222-2120-4,
14222-2251-5,
14222-2430-4,
14222-3000-5, view more14222-3000-6, 14222-7000-1
- Packager: Rodan & Fields
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 3, 2026
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
- Uses
- Warnings
- Directions
- Other information
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Inactive ingredients
hydrogenated polyisobutene, phenyl trimethicone, ethylhexyl palmitate, dextrin palmitate, helianthus annuus (sunflower) seed oil, caprylic/capric triglyceride, glyceryl behenate, disteardimonium hectorite, dipalmitoyl hydroxyproline, BHT, C10-18 triglycerides, calcium sodium borosilicate, capsicum annuum fruit extract, glyceryl dioleate, menthol, lactic acid, linoleic acid, linolenic acid, octyldodecanol, oleic acid, palmitic acid, palmitoyl tripeptide-1, polyhydroxystearic acid, sodium hyaluronate, sorbitan isostearate, sorbitan oleate, stearic acid, synthetic fluorphlogopite, tetrahexyldecyl ascorbate, tocopherol, tocopheryl acetate, tribehenin, triolein, may contain (+/-): blue 1 lake (Cl 42090), iron oxides (Cl 77491, Cl 77492, Cl 77499), red 6 (Cl 15850), yellow 5 lake (Cl 19140)
- Questions?
- SOOTHE Moisturizing Rescue Cream
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
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Inactive ingredients
aqua/water/eau, ascorbyl palmitate, behenic acid, butyrospermum parkii (shea) butter, C12-16 alcohols, calcium gluconate, caprooyl phytosphingosine, caprooyl sphingosine, caprylic/capric triglyceride, caprylyl glycol, ceramide AP, ceramide EOP, ceramide EOS, ceramide NP, ceramide NS, ceteareth-25, cetyl alcohol, cholesterol, curcuma wenyujin/curcuma kwangsiensis rhizome extract, cynara scolymus (artichoke) leaf extract, decyl glucoside, dimethicone, dipotassium glycyrrhizate, disodium EDTA, ethylhexylglycerin, gluconolactone, glycerin, helianthus annuus (sunflower) seed oil, hexylene glycol, hydrogenated lecithin, lecithin, maltodextrin, ophiopogon japonicus root extract, opuntia ficus-indica fruit extract, palmitic acid, panthenol, phenoxyethanol, polysilicone-11, potassium sorbate, propanediol, sodium acrylates copolymer, sodium benzoate, tocopherol, xanthan gum, yeast extract
- Questions?
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
When using this product
- skin irritation may occur, characterized by redness, burning, itching, peeling or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration.
- skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
- avoid unnecessary sun exposure and use a sunscreen
- avoid contact with the eyes, lips and mouth
- avoid contact with hair and dyed fabrics, which may be bleached by this product
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Directions
- clean the skin thoroughly before applying this product
- dispense 1-2 pumps from each side. Blend product evenly.
- cover the entire affected area with a thin even layer one to three times daily, as needed
- because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
- if bothersome dryness or peeling occurs, reduce application to once a day or every other day
- do not rinse product off face
- if going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.
- wash hands after application to help avoid staining fabrics
- Other information
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Inactive ingredients
allantoin, aloe barbadensis leaf juice, aminomethyl propanol, aqua/eau/water, benzyl alcohol, BHT, biosaccharide gum-1, C13-14 isoalkane, carbomer, ceramide AP, ceramide EOP, ceramide NP, chamomilla recutita (matricaria) flower extract, cholesterol, citronellol, corn starch modified, disodium EDTA, ethoxydiglycol, ethylhexylglycerin, fragrance/parfum, geraniol, glycerin, laureth-7, leuconostoc/radish root ferment filtrate, limonene, linalool, niacinamide, panthenol, PEG-7 glyceryl cocoate, phenoxyethanol, phytosphingosine, polyacrylamide, punica granatum fruit extract, sodium lauroyl lactylate, xanthan gum, yucca glauca root extract
- Questions?
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
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Uses
- helps prevent sunburn
- if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun
- Warnings
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Directions
- every AM, apply liberally and evenly over face + neck at least 15 minutes before sun exposure
- reapply at least every 2 hours
- use a water-resistant sunscreen if swimming or sweating
- Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m.-2 p.m.
- wear long-sleeved shirts, pants, hats and sunglasses
- children under 6 months of age: Ask a doctor
- Other information
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Inactive ingredients
1,2-hexanediol, alcohol denat., aluminum starch octenylsuccinate, water, benzoic acid, beta vulgaris (beet) root extract, biosaccharide gum-4, butylene glycol, butyloctyl salicylate, calcium gluconate, carnosine, cetearyl alcohol, cetyl ethylhexanoate, chlorphenesin, cynara scolymus (artichoke) leaf extract, dehydroacetic acid, diglycerin, dimethicone, dimethicone crosspolymer, disodium EDTA, disodium lauriminodipropionate tocopheryl phosphates, fragrance/parfum, fructooligosaccharides, gluconolactone, glycerin, HDI/trimethylol hexyllactone crosspolymer, hydrogenated polyisobutene, lactic acid, methyl carboxymethylphenyl aminocarboxypropylphosphonate, methyl methacrylate crosspolymer, niacinamide, pentylene glycol, phenoxyethanol, phragmites karka extract, polyacrylate-13, polyisobutene, polysorbate 20, poria cocos extract, potassium lactate, propanediol, red 33 (Cl 17200), silica, sodium acetylated hyaluronate, sodium benzoate, sodium chloride, sodium polyacryloyldimethyl taurate, sodium stearoyl glutamate, sorbitan isostearate, tocopherol, vitis vinifera (grape) juice extract, VP/eicosene copolymer, yellow 5 (Cl 19140)
- Questions?
- Principal Display Panel – Kit Carton Lavel
- Principal Display Panel – 5 mL Tube Label
- Principal Display Panel - 12 mL Tube Label
- Principal Display Panel - 8 mL Bottle Label
- Principal Display Panel - 30 mL Jar Label
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INGREDIENTS AND APPEARANCE
12 DAYS OF DERM-LOVED SKINCARE
octinoxate, zinc oxide, oatmeal, benzoyl peroxide, avobenzone, octisalate, octocrylene kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:14222-7000 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:14222-7000-1 1 in 1 CARTON; Type 1: Convenience Kit of Co-Package 10/01/2025 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 2 TUBE 10 mL Part 2 1 TUBE 12 mL Part 3 1 BOTTLE, PUMP 8 mL Part 4 1 JAR 30 mL Part 1 of 4 RODAN AND FIELDS PLUMPING LIP SPF 28 SUNSCREEN
octinoxate, zinc oxide oilProduct Information Item Code (Source) NDC:14222-3000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 7.4 g in 100 mL Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide 7 g in 100 mL Inactive Ingredients Ingredient Name Strength Hydrogenated Polyisobutene (1300 MW) (UNII: 7D1YQ9Y5EZ) Phenyl Trimethicone (UNII: DR0K5NOJ4R) Ethylhexyl Palmitate (UNII: 2865993309) Dextrin Palmitate (Corn; 20000 MW) (UNII: 89B2BSF9I3) Sunflower Oil (UNII: 3W1JG795YI) Medium-Chain Triglycerides (UNII: C9H2L21V7U) Glyceryl Monobehenate (UNII: A626UU0W2A) Disteardimonium Hectorite (UNII: X687XDK09L) Dipalmitoyl Hydroxyproline (UNII: E6AHA53N1H) Butylated Hydroxytoluene (UNII: 1P9D0Z171K) C10-18 Triglycerides (UNII: 43AGM4PHPI) Calcium Sodium Borosilicate (UNII: 4MM76N4WMY) Glyceryl Dioleate (UNII: Z3MP1W91CW) Menthol (UNII: L7T10EIP3A) Lactic Acid (UNII: 33X04XA5AT) Linoleic Acid (UNII: 9KJL21T0QJ) Linolenic Acid (UNII: 0RBV727H71) Octyldodecanol (UNII: 461N1O614Y) Oleic Acid (UNII: 2UMI9U37CP) Palmitic Acid (UNII: 2V16EO95H1) Palmitoyl Tripeptide-1 (UNII: RV743D216M) Hyaluronate Sodium (UNII: YSE9PPT4TH) Sorbitan Isostearate (UNII: 01S2G2C1E4) Sorbitan Monooleate (UNII: 06XEA2VD56) Stearic Acid (UNII: 4ELV7Z65AP) Magnesium Potassium Aluminosilicate Fluoride (UNII: YK3DC63Y5M) Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ) Tocopherol (UNII: R0ZB2556P8) .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0) Tribehenin (UNII: 8OC9U7TQZ0) Glyceryl Trioleate (UNII: O05EC62663) FD&C Blue No. 1 Aluminum Lake (UNII: J9EQA3S2JM) FERRIC OXIDE RED (UNII: 1K09F3G675) D&C Red No. 6 (UNII: 481744AI4O) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:14222-3000-5 5 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:14222-3000-6 5 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 05/16/2024 Part 2 of 4 SOOTHE MOISTURIZING RESCUE CREAM
oatmeal creamProduct Information Item Code (Source) NDC:14222-2430 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y) OATMEAL 0.01 g in 1 mL Inactive Ingredients Ingredient Name Strength ASCORBYL PALMITATE (UNII: QN83US2B0N) BEHENIC ACID (UNII: H390488X0A) SHEA BUTTER (UNII: K49155WL9Y) C12-16 ALCOHOLS (UNII: S4827SZE3L) CALCIUM GLUCONATE (UNII: SQE6VB453K) N-HEXANOYLSPHINGOSINE (UNII: 038753E78J) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CERAMIDE AP (UNII: F1X8L2B00J) CERAMIDE 1 (UNII: 5THT33P7X7) 3-DEHYDROXY CERAMIDE 1 (UNII: CR0J8RN66K) CERAMIDE NP (UNII: 4370DF050B) CERAMIDE NG (UNII: C04977SRJ5) CETEARETH-25 (UNII: 8FA93U5T67) CETYL ALCOHOL (UNII: 936JST6JCN) CHOLESTEROL (UNII: 97C5T2UQ7J) CURCUMA KWANGSIENSIS ROOT (UNII: 2WSI2681TI) CYNARA SCOLYMUS LEAF (UNII: B71UA545DE) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLUCONOLACTONE (UNII: WQ29KQ9POT) GLYCERIN (UNII: PDC6A3C0OX) SUNFLOWER OIL (UNII: 3W1JG795YI) HEXYLENE GLYCOL (UNII: KEH0A3F75J) HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) MALTODEXTRIN (UNII: 7CVR7L4A2D) OPHIOPOGON JAPONICUS ROOT (UNII: 90PS6JV9GZ) PRICKLY PEAR FRUIT (UNII: 18V8PAQ629) PALMITIC ACID (UNII: 2V16EO95H1) PANTHENOL (UNII: WV9CM0O67Z) PHENOXYETHANOL (UNII: HIE492ZZ3T) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) PROPANEDIOL (UNII: 5965N8W85T) SODIUM BENZOATE (UNII: OJ245FE5EU) TOCOPHEROL (UNII: R0ZB2556P8) WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:14222-2430-4 12 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 06/01/2021 Part 3 of 4 UNBLEMISH DUAL INTENSIVE ACNE TREATMENT
benzoyl peroxide lotionProduct Information Item Code (Source) NDC:14222-2120 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE 0.025 g in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) GLYCERIN (UNII: PDC6A3C0OX) POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) ALLANTOIN (UNII: 344S277G0Z) ALOE VERA LEAF (UNII: ZY81Z83H0X) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) BENZYL ALCOHOL (UNII: LKG8494WBH) BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) CERAMIDE 1 (UNII: 5THT33P7X7) CERAMIDE AP (UNII: F1X8L2B00J) CERAMIDE NP (UNII: 4370DF050B) CHOLESTEROL (UNII: 97C5T2UQ7J) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GERANIOL (UNII: L837108USY) LAURETH-7 (UNII: Z95S6G8201) LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458) LIMONENE, (+)- (UNII: GFD7C86Q1W) LINALOOL, (+/-)- (UNII: D81QY6I88E) MATRICARIA CHAMOMILLA FLOWERING TOP (UNII: 3VNC7T6Z02) NIACINAMIDE (UNII: 25X51I8RD4) PANTHENOL (UNII: WV9CM0O67Z) PEG-7 GLYCERYL COCOATE (UNII: VNX7251543) PHENOXYETHANOL (UNII: HIE492ZZ3T) PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q) POMEGRANATE (UNII: 56687D1Z4D) SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO) STARCH, CORN (UNII: O8232NY3SJ) XANTHAN GUM (UNII: TTV12P4NEE) YUCCA GLAUCA ROOT (UNII: 1A15YBH7N1) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:14222-2120-4 8 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 10/01/2025 Part 4 of 4 REDEFINE TRIPLE DEFENSE
avobenzone, octisalate, octocrylene creamProduct Information Item Code (Source) NDC:14222-2251 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 0.07 g in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 0.05 g in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 0.03 g in 1 mL Inactive Ingredients Ingredient Name Strength 1,2-HEXANEDIOL (UNII: TR046Y3K1G) ALCOHOL (UNII: 3K9958V90M) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) WATER (UNII: 059QF0KO0R) BENZOIC ACID (UNII: 8SKN0B0MIM) BETA VULGARIS (UNII: 4G174V5051) BIOSACCHARIDE GUM-4 (UNII: 9XRL057X90) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) CALCIUM GLUCONATE (UNII: SQE6VB453K) CARNOSINE (UNII: 8HO6PVN24W) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETYL ETHYLHEXANOATE (UNII: 134647WMX4) CHLORPHENESIN (UNII: I670DAL4SZ) CYNARA SCOLYMUS LEAF (UNII: B71UA545DE) DEHYDROACETIC ACID (UNII: 2KAG279R6R) DIGLYCERIN (UNII: 3YC120743U) DIMETHICONE (UNII: 92RU3N3Y1O) DIMETHICONE CROSSPOLYMER (450000 MPA.S) (UNII: UF7620L1W6) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) DISODIUM LAURIMINODIPROPIONATE TOCOPHERYL PHOSPHATES (UNII: 0K5Y9U1P6M) BETA VULGARIS ROOT FRUCTOOLIGOSACCHARIDES (UNII: N2UDM48ZD6) GLUCONOLACTONE (UNII: WQ29KQ9POT) GLYCERIN (UNII: PDC6A3C0OX) HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9) HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ) LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT) METHYL CARBOXYMETHYLPHENYL AMINOCARBOXYPROPYLPHOSPHONATE (UNII: K48QWH6YGJ) METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q) NIACINAMIDE (UNII: 25X51I8RD4) PENTYLENE GLYCOL (UNII: 50C1307PZG) PHENOXYETHANOL (UNII: HIE492ZZ3T) PHRAGMITES KARKA WHOLE (UNII: 10086A360Y) POLYACRYLATE-13 (UNII: FS2D4T67EA) POLYISOBUTYLENE (2300 MW) (UNII: DSQ2V1DD1K) POLYSORBATE 20 (UNII: 7T1F30V5YH) FU LING (UNII: XH37TWY5O4) POTASSIUM LACTATE (UNII: 87V1KMK4QV) PROPANEDIOL (UNII: 5965N8W85T) D&C RED NO. 33 (UNII: 9DBA0SBB0L) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM POLYACRYLOYLDIMETHYL TAURATE (UNII: NG5NG5733T) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) TOCOPHEROL (UNII: R0ZB2556P8) WINE GRAPE JUICE (UNII: JHQ6158A7R) EICOSYL POVIDONE (UNII: XQQ9MKE2BJ) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:14222-2251-5 30 mL in 1 JAR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 06/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 10/01/2025 Labeler - Rodan & Fields (051659584)





