Label: EQUATE BEAUTY DAY CREAM- ensulizole, octinoxate cream
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Contains inactivated NDC Code(s)
NDC Code(s): 49035-877-01 - Packager: Wal-Mart Stores, 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 July 5, 2017
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
WarningsSkin Cancer/Skin Aging Alert: Spending time in the sun increases your
risk of skin cancer and early sking aging. This product has been shown only to help
prevent sunburn, not skin cancer or early skin aging.
For external use only.
Do not use on •damaged or broken skin
When using this product •keep out of eyes. Rinse with wter to remove.
Stop use and ask a doctor •if rash occurs.
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
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INACTIVE INGREDIENT
Inactive ingredients water, cyclopentasiloxane, glycerin, mineral oil,
titanium dioxide, alumina, simethicone, glyceryl stearate, PEG-100 stearate,
myristyl myristate, triethanolamine, cetearyl alcohol, stearic acid, palmitic acid, PEG-20
stearate, phenoxyehtanol, ethylhexylglycerin, mannitol, cyclodextrin, yeast extract,
disodium succinate, panthenol (pro-vitamin B-5), polyacrylamide, C13-14 isoparaffin,
laureth-7, honey extract, soluble collagen, hydrolyzed elastin, sodium PCA, serine,
glycogen, butylene glycol, carbomer, polysorbate 20, palmitoyl tripeptide-1,
palmitoyl tripeptide-7, tocopherol acetate (vitamin E), polyacrylate-13,
polyisobutene, fragrance, allantoin, rosa canina fruit oil, salicylic acid, jasminum
officinale (jasmine) flower extract, glycine soja (soybean) protein, yellow 5
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
EQUATE BEAUTY DAY CREAM
ensulizole, octinoxate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-877 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42) ENSULIZOLE 1.19 g in 70 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 5.25 g in 70 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) GLYCERIN (UNII: PDC6A3C0OX) MINERAL OIL (UNII: T5L8T28FGP) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) ALUMINUM OXIDE (UNII: LMI26O6933) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) MYRISTYL MYRISTATE (UNII: 4042ZC00DY) TROLAMINE (UNII: 9O3K93S3TK) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) STEARIC ACID (UNII: 4ELV7Z65AP) PALMITIC ACID (UNII: 2V16EO95H1) PEG-20 STEARATE (UNII: NBX892EA57) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) MANNITOL (UNII: 3OWL53L36A) BETADEX (UNII: JV039JZZ3A) YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U) SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3) PANTHENOL (UNII: WV9CM0O67Z) POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) LAURETH-7 (UNII: Z95S6G8201) HONEY (UNII: Y9H1V576FH) MARINE COLLAGEN, SOLUBLE (UNII: 8JC99XGU4W) HYDROLYZED BOVINE ELASTIN (BASE; 1000 MW) (UNII: ZR28QKN0WT) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) SERINE (UNII: 452VLY9402) GLYCOGEN (UNII: 309GSC92U1) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) POLYSORBATE 20 (UNII: 7T1F30V5YH) PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M) PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52) ALLANTOIN (UNII: 344S277G0Z) ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ) SALICYLIC ACID (UNII: O414PZ4LPZ) JASMINUM OFFICINALE FLOWER (UNII: 0Q8K841432) SOY PROTEIN (UNII: R44IWB3RN5) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-877-01 1 in 1 CARTON 06/26/2017 1 70 g 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 not final part352 06/25/2017 Labeler - Wal-Mart Stores, Inc. (051957769)