Label: SECRET DIG aerosol, spray
- NDC Code(s): 84462-456-01, 84462-456-02
- Packager: Yiwu Mijue electronic Commerce Co., LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated June 26, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
WATER 45%
METHYLPARABEN 5%
BHT 2%
ISODODECANE 2%
ISOOCTANE 2%
DIBUTYL ADIPATE 1%
LAURYL PEG-10 TRIS(TRIMETHYLSILOXY)SILYLETHYL DIMETHICONE 1%
TOCOPHEROL 1%
POLYHYDROXYSTEARIC ACID 1%
BISABOLOL 1%
TOCOPHEROL 1%
PARFUM 1%
DIPOTASSIUM GLYCYRRHIZATE 1%
PHENOXYETHANOL 1%
ETHYLHEXYLGLYCERIN 1%
BUTYLENE GLYCOL 1%
OPUNTIA DILLENII EXTRECT 1%
AVENA SATIVA (OAT) BRAN EXTRACT 0.5%
OPHIOPOGON JAPONICUS ROOT EXTRACT 0.5%
PAEONIA LACTIFLORA ROOT EXTRACT 0.5%
SCUTELLARIA BAICALENSIS ROOT EXTRACT 0.5%
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PURPOSE
A lightweight sunscreen spray specially designed foroutdoor use can effectively block the exposure of UVA andUVB,evenly cover the skin, with fresh texture, and can breapplied at any time.lt is fresh and not greasy, and can formsunscreen isolation layer on the surface of the skin to providesunscreen care.
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SECRET DIG
secret dig aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84462-456 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 36 g in 100 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 36 g in 100 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 20 g in 100 g Inactive Ingredients Ingredient Name Strength DECYL GLUCOSIDE (UNII: Z17H97EA6Y) BISOCTRIZOLE (UNII: 8NT850T0YS) WATER (UNII: 059QF0KO0R) DEHYDROXANTHAN GUM (UNII: 63ZP7I1BQO) N-SALICYLOYLGLYCINE (UNII: 5BR3P7J05U) BEMOTRIZINOL (UNII: PWZ1720CBH) ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4) 2-PHENYLPROPANAL PROPYLENE GLYCOL ACETAL (UNII: 1ZRR9A405A) OCTOCRYLENE (UNII: 5A68WGF6WM) ZINC OXIDE (UNII: SOI2LOH54Z) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color white Score 2 pieces Shape FREEFORM Size 500mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84462-456-02 200 in 1 BOX 06/27/2024 1 NDC:84462-456-01 150 g in 1 BOTTLE, SPRAY; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product) Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/27/2024 Labeler - Yiwu Mijue electronic Commerce Co., LTD (413886387)
