Label: AMBRA GRISEA- ambergris liquid
- NDC Code(s): 71919-037-07, 71919-037-08, 71919-037-09, 71919-037-10
- Packager: Washington Homeopathic Products
- 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.
Updated December 30, 2018
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- ACTIVE INGREDIENTS
To relieve the symptoms of nervousness.Close
- KEEP OUT OF REACH OF CHILDREN
Keep this and all medicines out of reach of children.Close
- STOP USE AND ASK DOCTOR
If symptoms persist/worsen or if pregnant/nursing, consult your practitioner.Close
Adults: 4 drops into a tsp. of water 3 times a day. Children: 1/2 dose. Repeat at greater intervals as condition subsides. Or as directed bya lic. practitioner.Close
- INACTIVE INGREDIENTS
- PRINCIPAL DISPLAY PANEL
The OTC potency range of AMBRA is 2x–30x, 1c–30c, 200c, 1m, 10m, 50m, and CM.
Availability is subject to change.
All WHP single remedies are made to order; thus, the labels are printed on the same label stock, as the orders are filled.
‘Bottle Size,’ ‘Potency,’ and ‘Alcohol Percentage’ vary on the label depending on customer choice.
Standard bottle sizes for dilution-form remedies are 15ml, 30ml, 50ml, and 100ml.Close
- INGREDIENTS AND APPEARANCE
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71919-037 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMBERGRIS (UNII: XTC0D02P6C) (AMBERGRIS - UNII:XTC0D02P6C) AMBERGRIS 30 [hp_C] in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Product Characteristics Color white (white) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71919-037-07 15 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product 04/29/2010 2 NDC:71919-037-08 30 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product 04/29/2010 3 NDC:71919-037-09 50 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/29/2010 4 NDC:71919-037-10 100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/29/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/29/2010 Labeler - Washington Homeopathic Products (084929389) Establishment Name Address ID/FEI Business Operations Washington Homeopathic Products 084929389 manufacture(71919-037)