Label: NATURAL RELIEF 1222- bryonia 6x, rhus toxicodendron 6x lotion
- NDC Code(s): 76348-480-32
- Packager: RENU LABORATORIES, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated January 17, 2022
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- ACTIVE INGREDIENT
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WARNINGS
For external use only Avoid contact with eyes and open wounds. Stop use and ask a doctor if condition persists for more than 3 days or worsens. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Do not use this product if you are hypersensitive to any of the ingredients.
- PURPOSE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- STATEMENT OF IDENTITY
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INACTIVE INGREDIENT
Water, Cetearyl Alcohol, Ceteareth-20, Squalene, Propylene Glycol, Prunus Amygdalus Dulcis Oil, Glycine Soja Oil,
Stearic Acid, Tocopherol, Aloe Barbadensis Leaf Juice, SD Alcohol 40-B, Myristyl Myristate, Hydrolyzed Elastin, Hydrolyzed Keratin,
Allium Sativum Bulb Extract, Fragrance, Triethanolamine, Menthol USP, Phenoxyethanol, Benzoic Acid, Dehydroacetic Acid
- Natural Relief 1222 Label
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INGREDIENTS AND APPEARANCE
NATURAL RELIEF 1222
bryonia 6x, rhus toxicodendron 6x lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76348-480 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF 2.24 g in 224 g BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT 2.24 g in 224 g Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP) PHENOXYETHANOL (UNII: HIE492ZZ3T) GARLIC (UNII: V1V998DC17) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) MYRISTYL MYRISTATE (UNII: 4042ZC00DY) 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) MENTHOL (UNII: L7T10EIP3A) ALMOND OIL (UNII: 66YXD4DKO9) SOYBEAN OIL (UNII: 241ATL177A) ALOE VERA LEAF (UNII: ZY81Z83H0X) BENZOIC ACID (UNII: 8SKN0B0MIM) DEHYDROACETIC ACID (UNII: 2KAG279R6R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76348-480-32 896 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 02/20/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/20/2020 Labeler - RENU LABORATORIES, INC. (945739449) Establishment Name Address ID/FEI Business Operations Renu Laboratories, Inc. 945739449 manufacture(76348-480)