Label: FIELDTRIP - WHATEVER THE WEATHER DAILY MOISTURIZER ZINC OXIDE SUNSCREEN - SPF 30- zinc oxide lotion
- NDC Code(s): 66738-051-01, 66738-051-21
- Packager: Jack Black L.L.C
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 October 17, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
- Warnings
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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Directions
• Shake well before use
• Apply liberally 15 minutes before sun exposure
• Children under 6 months of age: Ask a doctor
• Reapply at least every 2 hours
• Use a water resistant sunscreen if swimming or sweating Sun Protection Measures. Spending time in the sun increasesyour risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF valueof 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.
- Other information
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INACTIVE INGREDIENT
Water, Caprylic/Capric Triglyceride, Butyloctyl Salicylate, Coco-Caprylate/Caprate, C12-15 Alkyl Benzoate, C14-22 Alcohols, Glycerin, Arachidyl Alcohol, Sodium Chloride, Withania Somnifera Root Extract, Sodium Hyaluronate, Acacia Senegal Gum, Jojoba esters, Behenyl Alcohol, Xanthan Gum, C12-20 Alkyl Glucoside, Fructose, Arachidyl Glucoside, Polyhydroxystearic Acid, Lecithin, Isostearic Acid, Polyglyceryl-3 Polyricinoleate, Polyisobutene, Polyacrylate-13, Polysorbate 20, Sorbitan Isostearate, Disodium EDTA, Phenoxyethanol, Ethylhexylglycerin. 21012
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
FIELDTRIP - WHATEVER THE WEATHER DAILY MOISTURIZER ZINC OXIDE SUNSCREEN - SPF 30
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66738-051 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 17.8 g in 100 mL Inactive Ingredients Ingredient Name Strength COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H) C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA) FRUCTOSE (UNII: 6YSS42VSEV) ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) POLYSORBATE 20 (UNII: 7T1F30V5YH) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) WATER (UNII: 059QF0KO0R) C14-22 ALCOHOLS (UNII: B1K89384RJ) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) SODIUM CHLORIDE (UNII: 451W47IQ8X) PHENOXYETHANOL (UNII: HIE492ZZ3T) ISOSTEARIC ACID (UNII: X33R8U0062) HYALURONATE SODIUM (UNII: YSE9PPT4TH) POLYISOBUTYLENE (1300 MW) (UNII: 241BN7J12Y) ACACIA (UNII: 5C5403N26O) XANTHAN GUM (UNII: TTV12P4NEE) JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL) DOCOSANOL (UNII: 9G1OE216XY) GLYCERIN (UNII: PDC6A3C0OX) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) WITHANIA SOMNIFERA ROOT (UNII: V038D626IF) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66738-051-01 1 in 1 CARTON 01/02/2023 1 NDC:66738-051-21 50 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 final M020 01/02/2023 Labeler - Jack Black L.L.C (847024036) Establishment Name Address ID/FEI Business Operations Northwest Cosmetic Laboratories, LLC D.B.A Elevation Labs Idaho 929572014 manufacture(66738-051)
