Label: TRADER JOES ZINC OXIDE MINERAL SUNSCREEN SPF 30- zinc oxide spray
- NDC Code(s): 71270-155-11
- Packager: Trader Joe's Company
- 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 January 12, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- KEEP OUT OF REACH OF CHILDREN
-
Directions
- Shake well
- Apply liberally 15 minutes before sun exposure.
- Reapply
- after 40 minutes of swimming or sweating
- immediately after towel drying
- at least every 2 hours.
- Spray on hands to apply to face. Do not inhale vapors.
- Use in a well-ventilated area
- Children under 6 months: ask a doctor.
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 15 value or higher along with 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.
- Other information
-
Inactive ingredients
ALOE BARBADENSIS LEAF JUICE, BENTONITE, BISABOLOL, BUTYLOCTYL SALICYLATE, CAPRYLHYDROXAMIC ACID, CAPRYLIC/CAPRIC TRIGLYCERIDE, CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER, CAPRYLYL GLYCOL, CELLULOSE GUM, CETEARYL ALCOHOL, CITRUS PARADISI (GRAPEFRUIT) PEEL OIL, COCO-GLUCOSIDE, ETHYL MACADAMIATE, GLYCERIN, JOJOBA ESTERS, METHYL DIHYDROABIETATE, MICROCRYSTALLINE CELLULOSE, OCTYLDODECYL OLEATE, PROPANEDIOL, SHEA BUTTER ETHYL ESTERS, SODIUM GLUCONATE, TOCOPHEROL, WATER.
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
TRADER JOES ZINC OXIDE MINERAL SUNSCREEN SPF 30
zinc oxide sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71270-155 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 15 g in 100 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) BENTONITE (UNII: A3N5ZCN45C) .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CARBOXYMETHYLCELLULOSE SODIUM (0.7 CARBOXYMETHYL SUBSTITUTION PER SACCHARIDE; 1200 MPA.S AT 1%) (UNII: 4J4P6L645M) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) GRAPEFRUIT PEEL (UNII: 3582N05Q44) COCO GLUCOSIDE (UNII: ICS790225B) ETHYL MACADAMIATE (UNII: ANA2NCS6V1) GLYCERIN (UNII: PDC6A3C0OX) HYDROGENATED JOJOBA OIL/JOJOBA OIL, RANDOMIZED (IODINE VALUE 40-44) (UNII: AS2SZ9757N) METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) OCTYLDODECYL OLEATE (UNII: MCA43PK7MH) PROPANEDIOL (UNII: 5965N8W85T) SHEA BUTTER (UNII: K49155WL9Y) SODIUM GLUCONATE (UNII: R6Q3791S76) TOCOPHEROL (UNII: R0ZB2556P8) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71270-155-11 171 g in 1 BOTTLE; Type 0: Not a Combination Product 04/02/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 04/02/2020 Labeler - Trader Joe's Company (006226666)
