HILL COUNTRY FARE MORNING FACIAL MOISTURIZING WITH BROAD SPECTRUM SPF 30 SUNSCREEN- homosalate, octocrylene, zinc oxide lotion

Hill Country Fare Morning Facial Moisturizing with Broad Spectrum SPF 30 Sunscreen by

Drug Labeling and Warnings

Hill Country Fare Morning Facial Moisturizing with Broad Spectrum SPF 30 Sunscreen by is a Otc medication manufactured, distributed, or labeled by H.E.B.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Homosalate 15.0%, Octocrylene 2.0%, Zinc Oxide 6.3%

Purpose

Sunscreen

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 use

• on damaged or broken skin

When using this product

• keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

• rash occurs.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• apply liberally 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

Other information

• protect the product in this container from excessive heat and direct sun
• may stain some fabrics

Inactive ingredients

aluminum starch octenylsuccinate, boron nitride, capryloyl glycine, carbomer, ceramide AP, ceramide EOP, ceramide NP, cetearyl alcohol, cetearyl glucoside, cetyl palmitate, cholesterol, dimethicone, disodium EDTA, ethylhexylglycerin, glycerin, hydroxyethylcellulose, niacinamide, phenoxyethanol, phytosphingosine, sodium hyaluronate, sodium lauroyl lactylate, sorbitan olivate, sorbitan palmitate, triethoxycaprylylsilane, undecylenoyl glycine, water, xanthan gum.

Labels

INGREDIENTS AND APPEARANCE

HILL COUNTRY FARE MORNING FACIAL MOISTURIZING WITH BROAD SPECTRUM SPF 30 SUNSCREEN 
homosalate, octocrylene, zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37808-939
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	6.3 mg  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	15 mg  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	2 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
XANTHAN GUM (UNII: TTV12P4NEE)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CERAMIDE AP (UNII: F1X8L2B00J)
CERAMIDE NP (UNII: 4370DF050B)
CETYL PALMITATE (UNII: 5ZA2S6B08X)
SORBITAN OLIVATE (UNII: MDL271E3GR)
CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
UNDECYLENOYL GLYCINE (UNII: 4D20464K2J)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
SORBITAN PALMITATE (UNII: 77K6Z421KU)
BORON NITRIDE (UNII: 2U4T60A6YD)
DIMETHICONE (UNII: 92RU3N3Y1O)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
WATER (UNII: 059QF0KO0R)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
NIACINAMIDE (UNII: 25X51I8RD4)
GLYCERIN (UNII: PDC6A3C0OX)
CERAMIDE 1 (UNII: 5THT33P7X7)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
POLYACRYLIC ACID (450000 MW) (UNII: KD3S7H73D3)
CHOLESTEROL (UNII: 97C5T2UQ7J)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37808-939-18	1 in 1 CARTON	11/18/2025
1	NDC: 37808-939-03	89 mL in 1 BOTTLE, PUMP; 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	11/18/2025

Labeler - H.E.B. (007924756)