Label: HALE AND HUSH BROAD SPECTRUM SPF 30 SPF 30- zinc oxide cream
- NDC Code(s): 83677-610-58
- Packager: Eclectic Solutions LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 20, 2023
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
-
Directions
- apply liberally 15 minutes before sun exposure
- use a water resistant sunscreen if swimming or sweating
- reapply at least every 2 hours
- 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 broad spectrum spf of 15 or higher and other sun protection measure including:
- limit time in the sun, especially from 10am to 2 pm
- wear long-sleeve shirts, pants, hats and sunglasses
- children under 6 months: Ask a doctor
-
INACTIVE INGREDIENT
Inactive Ingredients: Aqua (Water), Caprylic/Capric Triglyceride, Candelilla/Jojoba/Rice Bran Polyglyceryl-3 Esters, Glycerin, Isodecyl Neopentanoate, Ethyl Macadamiate, Aleurites Moluccanus Seed Oil, Hydroxypropyl Starch Phosphate, Glyceryl Stearate, Hamamelis Virginiana (Witch Hazel) Water, Ergothioneine [(L), Hordeum Distichon (Barley) Extract, Macadamia Ternifolia Seed Oil, Porphyra Umbilicalis (Red Algae) Extract, Santalum Album (Sandalwood) Extract, Phellodendron Amurense Bark Extract, Bisabolol (L-alpha), Glyceryl Isostearate, Sodium Stearoyl Lactylate, Polyglycery1-10 Pentastearate, Polyhydroxystearic Acid, Tocopheryl Acetate (D-alpha), Tocopherol (D-alpha), Lecithin, Malic Acid (L), Lonicera Caprifolium (Honeysuckle) Flower Extract, Lonicera Japonica (Honeysuckle) Flower Extract, Potassium Cetyl Phosphate, Hydrogenated Palm Glycerides, Alcohol, Cetearyl Alcohol, Behenyl Alcohol, Hydroxypropyl Methylcellulose, Sodium Lactate, Phytic Acid, Citric Acid, Sodium Hydroxide
- OTHER SAFETY INFORMATION
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
HALE AND HUSH BROAD SPECTRUM SPF 30 SPF 30
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83677-610 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 13.5 g in 100 g Inactive Ingredients Ingredient Name Strength PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G) POLYGLYCERYL-10 STEARATE (UNII: 90TF85HH91) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) MALIC ACID, L- (UNII: J3TZF807X5) PEG-60 GLYCERYL STEARATE (UNII: 85O35YN6YY) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) WITCH HAZEL (UNII: 101I4J0U34) DOCOSANOL (UNII: 9G1OE216XY) SODIUM LACTATE (UNII: TU7HW0W0QT) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) MACADAMIA OIL (UNII: 515610SU8C) CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9) ISODECYL NEOPENTANOATE (UNII: W60VYE24XC) ALEURITES MOLUCCANA SEED (UNII: J87WJ3E7VW) PORPHYRA UMBILICALIS (UNII: 14AN0J70WO) GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) HYPROMELLOSES (UNII: 3NXW29V3WO) ERGOTHIONEINE (UNII: BDZ3DQM98W) SANDALWOOD (UNII: 3641YW25N2) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) BARLEY (UNII: 5PWM7YLI7R) ALCOHOL (UNII: 3K9958V90M) LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U) HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q) LEVOMENOL (UNII: 24WE03BX2T) HYDROXYPROPYL CORN STARCH (5% SUBSTITUTION BY WEIGHT) (UNII: 9M44R3409A) ETHYL MACADAMIATE (UNII: ANA2NCS6V1) SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN) FYTIC ACID (UNII: 7IGF0S7R8I) SODIUM HYDROXIDE (UNII: 55X04QC32I) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83677-610-58 55 g in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 04/02/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 04/02/2018 Labeler - Eclectic Solutions LLC (068556928)