Pollen Guard Ragweed
- Product NDC
- 76097-003
- 11-digit product format
- 760970003
- Labeler code
- 76097
- Product ID
- 76097-003_a57dc676-bf56-4bd3-a285-5d81c3366213
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ambrosia Artemisiaefolia
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Western Allergy Services Ltd.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2011-10-03
- Marketing end
- 0000-00-00
- Substance
- AMBROSIA ARTEMISIIFOLIA
- Active strength
- 1 [hp_X]/5mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76097-003-05 | Pollen Guard RagweedRagweed Hay Fever Symptom Relief | 5 mL in 1 BOTTLE, UNIT-DOSE | LIQUID | 5 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76097-003 | POLLEN GUARD RAGWEED RAGWEED HAY FEVER SYMPTOM RELIEF (AMBROSIA ARTEMISIAEFOLIA) LIQUID [WESTERN ALLERGY SERVICES LTD.] | 1 | Legacy NDC, 1 package rows | 20111003_d8a9668e-5026-41e4-b594-078da152aa93.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 76097-003-05 | 76097000305 | 5 mL in 1 BOTTLE, UNIT-DOSE | 5 ml | Historical |