- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
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Inactive ingredients
Aloe barbadensis (aloe vera) extract, alpha-bisabolol, Argania spinosa (argan) kernel oil, benzyl alcohol, Butyrospermum parkii (shea) butter, caprylic/capric triglyceride, cetyl hydroxyethylcellulose, citric acid, ethylhexylglycerin, glycerin, heptyl undecylenate, Persea gratissima (avocado) oil, phenoxyethanol, polyglyceryl-3 dicitrate/stearate, potassium sorbate, Prunus amygdalus dulcis (sweet almond) oil, purified water, Simmondsia chinensis (jojoba) oil, tetrasodium EDTA, tocopherols, Zingiber officinale (ginger) root extract.
- Questions
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 237 mL Bottle Label
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INGREDIENTS AND APPEARANCE
EARTHS CARE ECZEMA
oatmeal lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24286-1571 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Oatmeal (UNII: 8PI54V663Y) (Oatmeal - UNII:8PI54V663Y) Oatmeal 1.8 g in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Ginger Oil (UNII: SAS9Z1SVUK) Aloe Vera Leaf (UNII: ZY81Z83H0X) Cetyl Hydroxyethylcellulose (350000 MW) (UNII: T7SWE4S2TT) Edetate sodium (UNII: MP1J8420LU) Glycerin (UNII: PDC6A3C0OX) Shea Butter (UNII: K49155WL9Y) Almond Oil (UNII: 66YXD4DKO9) Medium-Chain Triglycerides (UNII: C9H2L21V7U) Heptyl Undecylenate (UNII: W77QUB6GXO) Jojoba Oil (UNII: 724GKU717M) Avocado Oil (UNII: 6VNO72PFC1) .ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC) Argan Oil (UNII: 4V59G5UW9X) Tocopherol (UNII: R0ZB2556P8) Potassium Sorbate (UNII: 1VPU26JZZ4) Phenoxyethanol (UNII: HIE492ZZ3T) Ethylhexylglycerin (UNII: 147D247K3P) Benzyl Alcohol (UNII: LKG8494WBH) Anhydrous Citric Acid (UNII: XF417D3PSL) Product Characteristics Color WHITE (Off-white) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:24286-1571-8 237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/19/2018 2 NDC:24286-1571-1 2.9 mL in 1 POUCH; Type 0: Not a Combination Product 08/02/2019 3 NDC:24286-1571-2 12.4 mL in 1 JAR; Type 0: Not a Combination Product 02/28/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 11/19/2018 Labeler - DLC Laboratories, Inc. (093351930) Establishment Name Address ID/FEI Business Operations DLC Laboratories, Inc. 093351930 MANUFACTURE(24286-1571) , LABEL(24286-1571)