HILL COUNTRY ESSENTIALS- dimethicone lotion 
H.E.B

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.

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Hill Country Essentials Moisturizing Lotion

Active ingredients

Dimethicone 1.2%

Purpose

Skin Protectant

Uses

Warnings

For external use only

Do not use

• deep or puncture wounds • animal bites • serious burns

When using this product

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

Stop use and ask a doctor if

• condition worsens • symptoms last more than seven days or clear up and occur again within a few days

Keep out of reach of children.

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

Directions

Other information

Inactive ingredients

water, glycerin, distearyldimonium chloride, petrolatum, isopropyl palmitate, cetyl alcohol, avena sativa (oat) kernel flour, benzyl alcohol, sodium chloride.

Label

HEB87585E5F6

HILL COUNTRY ESSENTIALS 
dimethicone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-995
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE12 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)  
PETROLATUM (UNII: 4T6H12BN9U)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
OATMEAL (UNII: 8PI54V663Y)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-995-69236 mL in 1 TUBE; Type 0: Not a Combination Product07/22/2010
2NDC:37808-995-43532 mL in 1 BOTTLE; Type 0: Not a Combination Product08/29/2011
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34707/22/2010
Labeler - H.E.B (007924756)

Revised: 12/2022
Document Id: c6b82e99-53ed-b57b-e053-2995a90adac4
Set id: c51d8647-8af6-473a-b989-dfa6bfdc368d
Version: 3
Effective Time: 20221230
 
H.E.B