DailyMed label
Relieve Remedy No. 21
DailyMed label · Speer Laboratories, LLC · version 1
Key facts
| Product | Relieve Remedy No. 21 |
|---|---|
| Labeler | Speer Laboratories, LLC |
| Document type | HUMAN OTC DRUG LABEL |
| Active ingredients | APIS MELLIFERA, BLACK COHOSH, CANIS LUPUS FAMILIARIS MILK, CHAMAELIRIUM LUTEUM ROOT, CYCLAMEN PURPURASCENS TUBER, LYCOPODIUM CLAVATUM SPORE, MATRICARIA RECUTITA, PLATINUM, SEPIA OFFICINALIS JUICE, SODIUM CHLORIDE, STRYCHNOS IGNATII SEED, STRYCHNOS NUX-VOMICA SEED |
| Active ingredient UNIIs | 1NM3M2487K, 269XH13919, 451W47IQ8X, 49DFR088MY, 7S82P3R43Z, C88X29Y479, DQV54Y5H3U, G0R4UBI2ZZ, G39P120JQT, G728143D8Q, K73E24S6X9, QDL83WN8C2 |
| Route | ORAL |
| NDC package codes | 55926-0021-2 |
| Effective date | Jul 30, 2013 |
| Set ID | dd84c71a-173c-480c-8f69-27baa7296d95 |
At a glance
- 1–9 NDC package codes
- 10–99 Active ingredients
- 1–9 Manufacturing establishments listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About DailyMed drug labels
DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.
Source: U.S. National Library of Medicine (NLM), DailyMed · Source date: