SUN AND HONEY- zinc oxide cream

Sun and Honey by

Drug Labeling and Warnings

Sun and Honey by is a Otc medication manufactured, distributed, or labeled by Amara Ventures. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient                                       Purpose

Zinc Oxide 10%                                         sunscreen

PURPOSE

Uses

• helps prevent sunburn
• if used as directed with other sun protection measures (see directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

• For external use only. 
• Do not useon broken or damaged skin. 
• When using this product keep out of eyes. Rinse with water to remove. 
• Stop use and ask a doctor ifrash occurs.

KEEP OUT OF REACH OF CHILDREN

Directions

• apply generously and evenly 15 minutes before sun exposure
• reapply at least every 2 hours 
• use a water resistant sunscreen if swimming or sweating
• children under 6 months of age: 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 value of 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.

Inactive Ingredients

Aqua (Water), Tallow, Simmondsia Chinensis (Jojoba) Oil Jojoba Esters, Organic Propolis, Organic Cera Alba (Beeswax), Tocopherol (Vitamin E), Helianthus Annuus (Sunflower) Extract, Oryza Sativa (Rice) Bran Extract, Salix Alba (Willow Bark) Extract, Xanthan Gum, Glycerin, Gluconolactone & Sodium Benzoate (Geogard Ultra), Potassium Sorbate.

Other Information

• protect the product in this container from excessive heat and direct sun
• Do not use if the seal is broken

Questions? support@sunandhoney.co

Product label

INGREDIENTS AND APPEARANCE

SUN AND HONEY 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85432-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
TALLOW (UNII: 98HPY76U4W)
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL (UNII: 724GKU717M)
JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL)
PROPOLIS WAX (UNII: 6Y8XYV2NOF)
YELLOW WAX (UNII: 2ZA36H0S2V)
TOCOPHEROL (UNII: R0ZB2556P8)
SUNFLOWER SEED (UNII: R9N3379M4Z)
RICE BRAN (UNII: R60QEP13IC)
SALIX ALBA BARK (UNII: 205MXS71H7)
XANTHAN GUM (UNII: TTV12P4NEE)
GLYCERIN (UNII: PDC6A3C0OX)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85432-001-01	1 in 1 BOX	03/20/2025
1		100 g 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 Drug	M020	03/20/2025

Labeler - Amara Ventures (103833258)