Label: NATURAL RELIEF 1222- menthol lotion
- NDC Code(s): 76348-711-08
- Packager: RENU LABORATORIES, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 15, 2024
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- ACTIVE INGREDIENT
- WARNINGS
- PURPOSE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- STATEMENT OF IDENTITY
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INACTIVE INGREDIENT
Allium Sativum (Garlic) Bulb Extract, Aloe Barbadensis (Aloe) Leaf Extract, Benzoic Acid, Collagen, Dehydroacetic Acid, Deionized Water, Emulsifying Wax NF, Fragrance, Glycine Soja (Soybean) Oil, HPUS Bryonia 10x, HPUS Rhus Toxicodendron 10x, Hydolyzed Elastin (Powder), Mineral Oil, Myristyl Myristate, Phenoxyethanol, Propylene Glycol, USP, Prunus Amygdalus Dulcis (Sweet Almond Oil), Squalane, Stearic Acid, Triethanolamine, Vitamin E dl Alpha Tocopherol
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
- STATEMENT OF IDENTITY
- Natural Relief 1222 Label
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INGREDIENTS AND APPEARANCE
NATURAL RELIEF 1222
menthol lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76348-711 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 2.8 g in 224 g Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP) PHENOXYETHANOL (UNII: HIE492ZZ3T) GARLIC (UNII: V1V998DC17) TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) MYRISTYL MYRISTATE (UNII: 4042ZC00DY) BRYONIA ALBA ROOT (UNII: T7J046YI2B) SQUALANE (UNII: GW89575KF9) WHITE WAX (UNII: 7G1J5DA97F) WATER (UNII: 059QF0KO0R) TROLAMINE (UNII: 9O3K93S3TK) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) HYDROLYZED BOVINE ELASTIN (BASE; 1000 MW) (UNII: ZR28QKN0WT) MARINE COLLAGEN, SOLUBLE (UNII: 8JC99XGU4W) ALMOND OIL (UNII: 66YXD4DKO9) SOYBEAN OIL (UNII: 241ATL177A) ALOE VERA LEAF (UNII: ZY81Z83H0X) BENZOIC ACID (UNII: 8SKN0B0MIM) DEHYDROACETIC ACID (UNII: 2KAG279R6R) TETRASODIUM EDETATE DIHYDRATE (UNII: 3JGX4KKZ4A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76348-711-08 224 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 01/22/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 01/22/2024 Labeler - RENU LABORATORIES, INC. (945739449) Establishment Name Address ID/FEI Business Operations Renu Laboratories, Inc. 945739449 manufacture(76348-711)