Label: BAMBOO ROSEMARY cream
- NDC Code(s): 48951-2130-5
- Packager: Uriel Pharmacy 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 November 14, 2024
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- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
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WARNINGS
Warnings: FOR EXTERNAL USE ONLY.
Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains traces of lactose. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid
contact with eyes. Do not use if safety seal is broken or missing. - QUESTIONS
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INGREDIENTS AND APPEARANCE
BAMBOO ROSEMARY
bamboo rosemary creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-2130 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FORMICA RUFA (UNII: 55H0W83JO5) (FORMICA RUFA - UNII:55H0W83JO5) FORMICA RUFA 5 [hp_X] in 1 g ROSEMARY OIL (UNII: 8LGU7VM393) (ROSEMARY OIL - UNII:8LGU7VM393) ROSEMARY OIL 2 [hp_X] in 1 g EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (EQUISETUM ARVENSE TOP - UNII:1DP6Y6B65Z) EQUISETUM ARVENSE TOP 3 [hp_X] in 1 g VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (VISCUM ALBUM FRUITING TOP - UNII:BK9092J5MP) VISCUM ALBUM FRUITING TOP 3 [hp_X] in 1 g BAMBUSA VULGARIS WHOLE (UNII: WCD45M1BSK) (BAMBUSA VULGARIS WHOLE - UNII:WCD45M1BSK) BAMBUSA VULGARIS WHOLE 3 [hp_X] in 1 g TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5) TIN 7 [hp_X] in 1 g BOS TAURUS INTERVERTEBRAL DISC (UNII: 0A04Z76C13) (BOS TAURUS INTERVERTEBRAL DISC - UNII:0A04Z76C13) BOS TAURUS INTERVERTEBRAL DISC 5 [hp_X] in 1 g Inactive Ingredients Ingredient Name Strength SORBIC ACID (UNII: X045WJ989B) LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) WATER (UNII: 059QF0KO0R) CETYL ALCOHOL (UNII: 936JST6JCN) FRANKINCENSE OIL (UNII: 67ZYA5T02K) TEA TREE OIL (UNII: VIF565UC2G) LAVENDER OIL (UNII: ZBP1YXW0H8) CITRUS PARADISI SEED (UNII: 12F08874Y7) STEARIC ACID (UNII: 4ELV7Z65AP) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) MYRRH OIL (UNII: H74221J5J4) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-2130-5 60 g in 1 TUBE; Type 0: Not a Combination Product 09/01/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/01/2009 Labeler - Uriel Pharmacy Inc. (043471163) Establishment Name Address ID/FEI Business Operations Uriel Pharmacy Inc. 043471163 manufacture(48951-2130)